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<![CDATA[Auto req ID: 20294BR School/Unit: Harvard School of Public Health Department: Nutrition Union: 00 - Non Union, Exempt or Temporary Duties & Responsibilities: The Senior Data Management Programmer is responsible for overseeing flow of data for a major national study of breast cancer. S/he will interface with research investigators as well as Analysis Coordinators in database development, cleaning, and documentation to prepare for the analysis of study data. This individual will manage and oversee the flow of multiple waves of data from the time they are scanned to their incorporation into files for analysis. This includes the development of on-screen validation procedures for each participant questionnaire, coordinating batches of data through the validation and editing procedures, cross checking a participant's identity with previously reported demographic information, and merging files with data from previous years. Responsible for maintaining an up-to-date name and address file and creating lists for each mailing. Also maintain and upgrade the customized software to aid in tracking and entering information for disease and death follow-up. Prepare data subsets for analyses by researchers, students, or other statisticians, working with study personnel, senior data analysis staff and researchers. Document datasets provided to others, original statistical programs and checking work to the extent that another could locate files and programs, understand programs and readily check, rerun or update work performed. Maintain resources both within the analysis group and throughout the division (other programmers, analysts, data managers, researchers, codebooks, manuscript files, locations of data, procedures, software, etc.). Also serve as a resource for other members of the group and division in areas of study, programming, software or other expertise. Create interim reports and data summaries, using advanced techniques, to be used for a wide variety of study management decisions and processes. Also develop procedures and software used in data management in close coordination with other large cohort studies to ensure efficient and compatible systems. Please note that this position can be graded at the 57 level based on experience, and would also include working with greater independence, more extensive statistical analyses in collaboration with investigators and coordinating with related projects. PLEASE NOTE; This position is grant funded through 5/31/2014. Basic Qualifications: Bachelors degree and 3 or more years experience in computer applications to human research problems required. Also required: Knowledge of research methodology; Familiarity with statistical reasoning; Applications programming experience in SAS; Strong organizational skills; Technical aptitude for anticipating and resolving problems imposed by computers operating in a clinical research environment; Strong interpersonal skills; Ability to write succinct and coherent explanations of complex technical procedures. Additional Qualifications: MPH or MS in Epidemiology or Biostatistics. Pre-Employment Screening: Criminal<img src="http://www.jobtarget.com/c/includes/jvimg.cfm?site=2445&job=6583140"><a href="http://www.apply-for-job.net/c/jobclick.cfm?site=2445&job=6583140" rel="nofollow">Apply Here!</a>]]>

<![CDATA[Description: Working under the direction of staff engineers and scientists identify, evaluate, prevent and control contamination and project sites. Working both in the office and in the field inspecting and managing equipment, collecting water and soil samples, preparation of field and lab reports of data, preparation and tracking of Bills of Lading and coordinating the off-site transportation and disposal of contaminated soils, construction demolition materials and other waste streams. Assisting with regulatory compliance and other duties as needed. Experience: Minimum 2 years hands on experience in preparation of Bills of Lading, on-site treatment of contaminated soils, collecting soil and water samples for disposal, coordination with laboratory personnel, familiar with area disposal options, i.e landfills, recycling facilities, RCRA materials and other waste stream disposal. Candidate must possess precision, attention to detail and the ability to communicate with team members. Must be highly organized, self motivated and should be comfortable working both in the office and in the field. Education: Associate degree in Applied Science or B.S. preferred in chemistry, environmental science or engineering or equivalent experience. ]]>

<![CDATA[Healthcare software company seeks Reimbursement Expert to advise in multiple areas including... - Ability of providers to bill under different behavioral health codes (smoking cessation, diet counseling, etc.). - Remote monitoring reimbursement. - HITECH Act Meaningful Use provisions. - Medical Device health economics studies. Contract to start with potential to transition to full-time based on mutual interest. Please reply with resume.]]>

<![CDATA[OVERALL RESPONSIBILITIES Manages a portfolio of projects for the Genome Sequencing Platform, including genome sequencing projects as well as other types of sequencing projects. Manages all Platform aspects of projects, from shipment and receipt of sample to sequence data delivery. Ensures that projects are completed on time and within budget. Works independently to anticipate needs of project team and/or project stakeholders, including reporting on project status, preparing relevant materials for meetings, etc. Communicates project progress to both Platform and Program senior staff. Uses project management skills and knowledge of tracking and reporting systems to support Platform-wide special projects as needed. CHARACTERISTIC DUTIES • Initiates Project Management activities for all new projects. • Ensures that the Platform-specific needs of each sequencing project have been clearly identified; translates project needs into deliverables and timelines. • Manages communication with outside collaborators about project logistics such as delivery schedule and quality requirements for input and/or output materials. • Ensures that projects and activities adhere to institutional guidelines with regards to safety and regulatory compliance. • Identifies that appropriate funds are in place for planned Platform work. • Tracks financial status of individual projects relative to available budget; assesses future financial needs and alerts Senior Staff to potential shortfalls. • Ensures that projects are completed on time and on budget; manages changes in timelines, deliverables and budget as needed to meet scientific goals of project. • Creates special reports for Platform reporting, grant agencies and scientific collaborators or specific reports as needed. • Oversees all Special Sequencing Projects and delegates tasks to Project Coordinators. • Other related tasks as required. • B.S. in biology or related field, with at least 5 years relevant professional experience required. • At least 1 year experience coordinating or conducting projects in high throughout laboratory setting. • Experience with customer or client relations preferred. • Excellent oral, written, interpersonal and organizational skills required. • Must have the ability to interact with an interdisciplinary group including data analysts, computer scientists and laboratory biologists. The Broad Institute was launched to pioneer a new model of collaborative biomedical science that would transform medicine. To accomplish these goals, we have built an amazing team of talented Broadies who work together to realize this transformation. We are always looking for new Broadies to join our team and help us tackle important problems at the cutting edge of science. The Broad community includes professional scientists from many disciplines, administrative staff, and students. We seek to cultivate an interdisciplinary, goal-oriented work environment that unleashes scientific creativity and empowers our people to pursue ambitious and critical projects. Our work transcends traditional academic boundaries, giving Broad employees and affiliates access to an unparalleled biomedical research community across the Harvard and MIT communities and beyond. The Broad Institute is committed to providing its employees with a competitive compensation and benefits package. We recognize the need for our employees to have a balance between work and personal life. To that end, our benefit plans and options reflect our desire to promote an environment that supports the health, diversity, and general wellbeing of our employees. All Broadies also have access to world-class research and state of the art technology and are fully supported in their professional development, pushing the envelope for further growth. The Broad Benefits Program includes:  -   Medical: choice from 2 HMOs and 1 PPO.  Broad pays 80% of premiums. -   Dental: 1 enriched plan.  Broad pays 80% of the premiums. -   Basic Life Insurance, Accidental Death & Dismemberment, Business Travel paid in full by Broad -   Supplemental Life Insurance choices for yourself, your spouse and children -   Short-Term and Long-Term Disability paid in full by Broad -   Flexible Spending Accounts, Health care, Dependent care, Parking, and Biking -   401(K) Plan w/ 6% Employer Match, and Annual Contribution (discretionary but targeted at 4% for 2010) -   4 Weeks of Vacation after 1 Year -   Tuition Reimbursement -   1 class each semester at MIT/Harvard paid in full (2 per year maximum) -   Identity Theft Prevention and Insurance paid in full by Broad -   Estate Planning - free will preparation -   Adoption Assistance -   Employee Assistance Program (EAP) -   MBTA Commuter & Transportation Subsidies (50% up to the federal maximum) -   Subsidized onsite parking, occasional parking, van pool, and car pool programs available -   Parents in a Pinch Back Up Child and Elder Care -   Credit Union -   Discounted Fitness and Gym memberships -   Pet Insurance -   Group Home & Auto Insurance -   Group Legal Program The Broad Institute is an equal opportunity employer. To learn more about the Broad’s job opportunities, visit our Career Center at: <a href="https://www.broadinstitute.org/careers/career-center" rel="nofollow">https://www.broadinstitute.org/careers/career-center</a> If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=873936-1857-8439" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=873936-1857-8439</a> ]]>

<![CDATA[Must have at least a B.Sc. degree in biological sciences, preferably in biochemistry with a good understanding of protein and DNA. Previous work experience in a research laboratory is highly preferred. The position requires some molecular biology techniques such as basic PCR, cloning, plasmid DNA preparation; growing bacteria culture and maintaining insect cell culture for protein expression; and protein purification using affinity resins and column chromatography. Tissue culture experience is a valuable asset.]]>

<![CDATA[We are seeking a Manufacturing Associate with experience in the biotechnology field to work in the Burlington, MA area. Job responsibilities will include cell culture, CIP, SIP, working with SOP's and batch records. 1-4 years industry experience is required.]]>

<![CDATA[JOB OPPORTUNITY – TECHNICAL SALES REPRESENTATIVE IBIDI, LLC ibidi, LLC, a leader in providing solutions for BioMicroscopy, is looking to add a new Technical Sales Representative to the US team. ibidi is an international company which began in Munich Germany and has greatly expanded in the US. We are looking for a motivated and technical individual to help grow and manage new territories in the East and/or West Coast market. This position is geared towards someone who is dedicated to life sciences and research but is more suited to work in the field rather than the lab. The successful candidate will be a self-starter with strong communication skills as well as a forward thinker. This is an amazing opportunity to work for an innovative and fast growing company and correct individual will be provided the tools and support to advance quickly. If interested, please see the extended job description below and send your Cover Letter, CV along with salary requirements to Megan Nicholson at mnicholson@ibidi.com. Relocation to the Madison, WI area is required for a training period To learn more about ibidi, please go to www.ibidi.com Technical Sales Representative ibidi LLC is an innovative company located in Verona, Wisconsin that specializes in solutions for BioMicroscopy. Our distinct line of products is primarily used in cell culture and high resolution microscopy for the advancement of stem cell research, cancer research, live cell imaging, chemotaxis, wound healing, angiogenesis and other cutting edge biotechnologies. ibidi’s broad range of micro-fluidic slides (µ- Slides), universal heating stages, flow pumps and other laboratory products are at work in the most sophisticated industrial, pharmaceutical, academic, clinical and biotech research institutions across the nation. We are currently seeking a highly motivated and dependable individual to join our sales team in Verona, WI as a Technical Sales Representative. Relocation to the Madison/Verona WI area is required for a training period. Upon completion of training there will be the opportunity to relocate to the East or West Coast to continue market development. The primary responsibilities will be to maintain a high level of product knowledge, generate leads, develop opportunities, negotiate/close high dollar sales, maintain existing customer relations and expand ibidi’s exposure in a highly competitive market. Excellent interpersonal, organizational, written and verbal communication skills are essential. This position requires about ¼ to ½ of the time spent on travel throughout the United States. Requirements: · Bachelor’s degree (Medical Science, Biology, or related field of study preferred) · Strong ability to develop and maintain customer relationships through inside sales · Strong analytical, organizational and project management skills · Ability to work independently to achieve monthly goals · Ability to identify business opportunities in relation to growth strategies · Represent ibidi LLC at scientific meetings, conventions and industry functions as needed · Intermediate to advanced MS Word and Excel skills · Sales experience is a plus · Lab experience is a plus Key Responsibilities: Customer visits and analysis of current and future needs Technical support to current customers and prospects Acquisition of new customers Organization of onsite demonstrations, exhibitions and workshops Develop key relationships in East and/or West Coast market If you are a motivated individual looking for professional growth and enjoy working in a fast paced environment, send your CV and salary history to: mnicholson@ibidi.com ibidi LLC is an Equal Opportunity Employer ]]>

<![CDATA[Requirements: Experience working in a laboratory with antibodies and related reagents; Experience must include significant and consistent experience in Western Blotting and one other antibody-related application (FACS, ELISA, immunohistochemistry, ChIP, ICC) MS in a life sciences field with 3 years experience, or BS in a life sciences field with 5 years experience Excellent problem solving skills Effective written and spoken English communication Extensive experience and comfort using computers, working knowledge of Excel, Powerpoint, and Outlook Responsibilties: Answer some pre-sale enquiries and extensive customer questions and complaints by phone and email Liaise with product suppliers to obtain product information when necessary Review product feedback from customers Updating product datasheets when new information becomes available Meet weekly to discuss issues that have arisen during the past week, give updates on progress, and discuss performance Occasional opportunities for travel to conferences and trade shows This is NOT a lab bench position. Responsibilities primarily include phone and email technical support. Candidates must live locally and be a US Citizen or Permanent Resident Green Card Holder Please submit resume as word attachment to jobs@cwsciences.com Commonwealth Sciences, Inc. www.cwsciences.com ]]>

<![CDATA[We are looking for Microbiology Dept Manager. You must meet or exceed AIHA-LAP requirements. Please respond with resume and salary requirements. Thank you. AIHA Technical Manager Requirements: The requirements for qualifying for technical manager for the AIHA-LAP, LLC Environmental Microbiology Laboratory Accreditation Program (EMLAP) are set forth in Policy Module 2D, Section 2D.4.1 (in addition to those in Module 2A). In order to qualify for Technical Manager (2.D.4.1.1), the candidate must have a Microbiology or life science degree (with eight (8) semester hours in microbiology), with three (3) years relevant non-academic work experience. A minimum of two (2) years experience must be in microbiological analyses within the scope of accreditation. The remaining one (1) year can be from other laboratory analytical procedures.]]>

<![CDATA[Would you like to succeed in an environment that encourages a healthy and rewarding work/life balance? Then consider working for Harvard Clinical Research Institute, Inc. (HCRI). As a leading academic clinical research organization, HCRI’s mission is to improve health and quality of life by collaborating with academic and industry partners to conduct high quality clinical research in a professionally nurturing and world-class academic environment. HCRI is continuing its expansion and currently has an opening for Regulatory Documents Coordinator who will be responsible for coordinating various levels of the daily functions associated with clinical site management. Primary Duties: · Coordinate activities as related to the conduct of all phases of pharmaceutical, biotechnology and medical device clinical trials. · Maintenance of departmental standard operational procedures and guidelines. · Collection, review, maintenance of regulatory documents from clinical sites. · Creation and distribution of regulatory packets and Investigator Binders to investigative sites. · Develop and maintain databases for tracking of regulatory documents, work flow process and other trial related documents. · Review Informed Consent forms and other study specific forms. · Generate and maintain study specific trial master files. · Organize and preparation of trial related material and presentations for Investigator and/or coordinator meetings. · Work with Clinical Site Manager and Sponsor in identifying and screening qualifications of appropriate investigative sites. · Help to maintain a site/investigator selection system/process. · Provide centralized site support and coordination to assure accurate and timely completion of all contracted activities. · Provide ongoing site management support through project completion. · Clinical trials research experience through exposure to protocols in a variety of therapeutic areas. · Knowledge of internal SOP’s, FDA/ICH guidelines to GCP’s and regulatory compliance. · Able to work independently and in a team environment. · Facilitate communication among the research centers, HCRI project teams, sponsors, site monitors vendors. Secondary Duties: Coordinate internal and external meetings Take and distribute meeting minutes Type correspondence Direct calls to the appropriate resources Review mail/distribute/fax correspondence Large mailings (reports, forms, etc;) Edit and/or review newsletters Requirements: Education: Required: BA or BS Preferred: BS in Life Sciences Yrs. of related experience: Required: None Preferred: 2 years of Clinical Trial and (primarily) Regulatory Experience Must be knowledgeable about computers and data management systems and familiar with common software packages (Word, Excel, PowerPoint, Outlook) and Internet communication. Must have the ability to prioritize multiple, competing tasks and demands and seek supervisory or other assistance when appropriate. Must have the ability to complete tasks in an accurate and timely manner. Needs to pay high attention to detail. Benefits: HCRI is committed to excellence and competence and affords an environment of professional development and education that enhances the personal growth of its employees. HCRI also offers a full range of benefits including subsidized parking; discounted T passes; health, dental and vision insurances; 3 weeks paid vacation; flex time; paid personal / sick time; 401K with employer match; pension plan; short and long term disabilities; tuition reimbursement; a convenient location, and more! HCRI is an equal opportunity employer that values the strength diversity brings to the workplace. ]]>

<![CDATA[Since a large number of applications is expected, reply only if your profile matches the requirements. Laboratory is looking for a full-time skilled Research Technician who will assist with research in the area of neuroscience, pharmacology and behavior and participate in preclinical research studies on addiction and stress-related disorders in rodents. Perform rat handling, behavioral tests (such as operant conditioning), intracranial surgeries and drug administrations; maintain rodent colonies. Perform experiments using such techniques as histology, immunohistochemistry, RT-PCR, DNA electrophoresis and western blot. Maintain the laboratory and order supplies. Requirements: We are especially looking for a motivated person ABLE TO WORK ALSO DURING THE WEEKENDS. CLOCK WATCHERS ARE NOT ENCOURAGED TO APPLY. Bachelors Degree in biological sciences, neuroscience or psychology is required, with 1-3 years of research experience. SOME EXPERIENCE WITH RODENTS REQUIRED; proficiency with some of the molecular techniques desired. Strong organizational skills, including the ability to handle a variety of tasks simultaneously and attention to details are required. Must be able to work independently. A 2-month (paid) test period might be contemplated. Interested applicants please send CV and cover letter by email; please mention expected salary range. Salary dependent on experience. Job Location: Boston University School of Medicine, Boston, MA ]]>

<![CDATA[Under specific direction, the Research Assistant will perform or participate in gene expression analysis in Human Leukocytes within the Immunological Genome Project. Principal duties include the fluorescent staining and purification of cells by flow cytometry, RNA extraction and purification, measurement of specific gene expression (qPCR, or other technologies). Liaise with the microarray core facility for sample flow and tracking. Coordinate with project immunologists in the definition of Standard Operating Protocols. Participate in data entry and management within study databases, and in the computational analysis of data generated in the project, in relation with project specialists or immunologists. Assist in the management of lab stocks, ordering of reagents and general lab maintenance. This is a grant funded position through September 30, 2011. Basic Qualifications: College background or equivalent work experience, and familiarity with standard computer usage. At least one year related work experience (relevant coursework may count towards experience). Additional Qualifications: A foundation in immunology and in particular flow cytometry; familiarity with molecular biology techniques; experience in gene expression analysis or in bioinformatics; demonstrated abilities in basic laboratory techniques helpful; good communication, organizational, and interpersonal skills; ability to take specific direction and work independently as appropriate, within specific guidelines. All applicants must apply via our website: www.employment.harvard.edu. Please type in 20402BR in the Auto Req ID field. <a href="http://www.employment.harvard.edu/" rel="nofollow">http://www.employment.harvard.edu/</a> Harvard University is an Affirmative Action/Equal Opportunity Employer]]>

<![CDATA[T2 Biosystems, Inc. is an exciting early stage company whose mission is to revolutionize diagnostic medicine by providing immediate, accurate testing for nearly any health condition, in nearly any setting. We are seeking a talented and highly motivated Scientist to join our Assay Development Group. If you have experience in the in vitro diagnostics industry, this could be a very exciting position for you. Responsibilities will broadly include using T2’s proprietary technology to develop a variety of quantitative IVD immunoassays to meet both FDA and EU regulatory requirements . You will apply your laboratory skills and experience in all phases of IVD product development; concept, feasibility, design and development, verification and validation, manufacturing transfer and commercialization. You will have: 5+ years of experience in commercial IVD assay development; a Bachelor’s degree in Clinical Lab Science, Biology, Biochemistry or related fields broad experience in all phases of immunoassay development including; applying DOE principles preparing and executing test plans adapting CLSI protocols and implementing appropriate statistical analysis demonstrated productivity in a laboratory setting; and excellent oral and written communication skills In addition, You must have excellent organizational, record keeping and communication skills. A strong work ethic to generate high quality data under tight deadlines, collaborative and proactive attitude a must. Prior experience in a fast-paced, entrepreneurial environment is a plus. You will be working on multiple, simultaneous projects, so it is important that you be able to manage time, interact with a variety of people, and adapt to rapid changes. To apply, please send your résumé and cover letter to careers@t2biosystems.com, and write the job title in the subject line. T2 Biosystems is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, gender, pregnancy, national origin, age, military service eligibility, veteran status, sexual orientation, marital status, disability, or any other protected class. ]]>

<![CDATA[T2 Biosystems, Inc. is an exciting early stage company whose mission is to revolutionize diagnostic medicine by providing immediate, accurate testing for nearly any health condition, in nearly any setting. We are seeking a talented and highly motivated Senior Research Associate to join our Assay Development Group. If you have experience in the in vitro diagnostics industry, this could be a very exciting position for you. Responsibilities include using T2’s proprietary technology to develop quantitative IVD immunoassays to meet both FDA and EU regulatory requirements . You will apply your laboratory skills and experience in all phases of IVD product development; concept, feasibility, design and development, verification and validation, manufacturing transfer and commercialization. You will have: 3+ years of experience in commercial IVD assay development; a Bachelor’s degree in Clinical Lab Science, Biology, Biochemistry or related fields; experience in all phases of immunoassay development; demonstrated productivity in a laboratory setting; and excellent oral and written communication skills In addition, You must have excellent organizational, record keeping and communication skills. A strong work ethic to generate high quality data under tight deadlines, collaborative and proactive attitude a must. Prior experience in a fast-paced, entrepreneurial environment is a plus. You will be working on multiple, simultaneous projects, so it is important that you be able to manage time, interact with a variety of people, and adapt to rapid changes. To apply, please send your résumé and cover letter to careers@t2biosystems.com, and write the job title in the subject line. T2 Biosystems is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, gender, pregnancy, national origin, age, military service eligibility, veteran status, sexual orientation, marital status, disability, or any other protected class. ]]>

<![CDATA[JOB TITLE: Chemical Technician RESPONSIBILITIES: Operation of monomer and polymer pilot plants, including material handling, reactions, distillation, and byproduct takeoff Analysis and characterization of samples Attention to detail critical with good laboratory skills Maintain records of experiments. Communicate results to others. Follow instructions, maintain a safe working environment and comply with all regulations. Flexible working hours, Monday through Saturday, including night and evening shifts. QUALIFICATIONS: · Previous experience in a laboratory setting or chemical manufacturing operation · Familiar with laboratory equipment and procedures · Excellent verbal and written communication skills · Basic mechanical / troubleshooting skills · Technical training in chemistry or engineering or equivalent prior experience. · Able to work independently and as part of team ]]>

<![CDATA[ RESEARCH ASSOCIATE: Formulations Department DUTIES: Assist the Scientist and other team members in development of formulation and pharmaceutical manufacturing process. Participate in the design of experiments and execution. Co-ordinate with formulation team members to arrange the equipment and room for experiments. Follow safety procedures to set up, operate and maintain equipment in formulation development laboratory Collect, track and archive development information Assist in preparation of technical protocols and reports. Experience with solid and liquid dosage form development SKILLS: Well organized, strong technical skills, good written and verbal communication skills, good computer skills and ability to multitask. Experience in Pharma would be preferred.Experience with solid and liquid dosage form development EDUCATION: Bachelors degree and 2 - 5 years or Masters and 0 - 2 years. ]]>

<![CDATA[As a member of the Chemical Biology Program, the Research Associate II will be involved in the synthesis, optimization and execution of libraries of biologically relevant small molecules. Research Associates are expected to work closely with Research Chemist II. Performs research and/or development in collaboration with others for projects. Makes detailed observations, analyzes data and interprets results. Investigates, creates and develops new methods and technologies for project advancement. Contributes to various projects to support the overall research goals and communicates effectively with all levels of staff and external collaborators to ensure that work supports team goals. Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. The specific focus of each experiment and the type of techniques employed may vary in accordance with shifts in team goals in a fast paced and dynamic environment. The location of this position is within the Department of Chemistry and Chemical Biology at Harvard University; however, some duties will be carried out at the Broad Institute. CHARACTERISTIC DUTIES • Works collaboratively with other scientists in optimizing or developing new synthetic pathways. • Performs follow-up medicinal chemistry for various collaborators of the Chemical Biology Program. • Conducts solid-phase library synthesis and/or parallel solution-phase synthesis. • In consultation with supervisor, responsible for independent design and implementation of experiments to address specific questions defined by group projects. • Makes detailed observations, analyzes data and interprets results. • Investigates, creates and develops new methods and technologies for project advancement. • Generates oral and written reports on performed experiments. Attends team meetings for experimental planning and present the results in project meetings. May participate in scientific conferences and contribute to scientific journals. • Manages changes in timelines and deliverables as needed to meet project goals. • May contribute to the identification of patentable inventions. • Consults with literature and other scientific staff as needed to maintain high level of professional expertise • Determines methods and procedures on new assignments. • May provide guidance to Research Technicians. • Other tasks as required or necessitated by the position. • Bachelors or Masters degree in Chemistry or related field required, or equivalent combination of education and experience. • Must possess at least 1-2 years of experience with solution phase organic synthesis, 1H NMR and analytical techniques such as TLC are required. Experience with 2D NMR, reverse and normal phase HPLC, SFC, LC-MS and solid phase synthesis are desirable. • Scientific expertise in analytical and synthetic organic chemistry including various methods of purification; knowledge of medicinal chemistry a plus. • Proficiency with SciFinder is desirable. • Must be able to solve complex problems in a creative and effective way. • Must demonstrate the ability to exercise judgment within broadly defined practices and techniques. • Excellent communication skills and the ability to interact professionally with all levels of staff and with external contacts in a fast paced environment required. • Exceptional organizational and critical thinking skills, lab notebook practices and attention to detail are essential.The Broad Institute was launched to pioneer a new model of collaborative biomedical science that would transform medicine. To accomplish these goals, we have built an amazing team of talented Broadies who work together to realize this transformation. We are always looking for new Broadies to join our team and help us tackle important problems at the cutting edge of science. The Broad community includes professional scientists from many disciplines, administrative staff, and students. We seek to cultivate an interdisciplinary, goal-oriented work environment that unleashes scientific creativity and empowers our people to pursue ambitious and critical projects. Our work transcends traditional academic boundaries, giving Broad employees and affiliates access to an unparalleled biomedical research community across the Harvard and MIT communities and beyond. The Broad Institute is committed to providing its employees with a competitive compensation and benefits package. We recognize the need for our employees to have a balance between work and personal life. To that end, our benefit plans and options reflect our desire to promote an environment that supports the health, diversity, and general wellbeing of our employees. All Broadies also have access to world-class research and state of the art technology and are fully supported in their professional development, pushing the envelope for further growth. The Broad Benefits Program includes:  -   Medical: choice from 2 HMOs and 1 PPO.  Broad pays 80% of premiums. -   Dental: 1 enriched plan.  Broad pays 80% of the premiums. -   Basic Life Insurance, Accidental Death & Dismemberment, Business Travel paid in full by Broad -   Supplemental Life Insurance choices for yourself, your spouse and children -   Short-Term and Long-Term Disability paid in full by Broad -   Flexible Spending Accounts, Health care, Dependent care, Parking, and Biking -   401(K) Plan w/ 6% Employer Match, and Annual Contribution (discretionary but targeted at 4% for 2010) -   4 Weeks of Vacation after 1 Year -   Tuition Reimbursement -   1 class each semester at MIT/Harvard paid in full (2 per year maximum) -   Identity Theft Prevention and Insurance paid in full by Broad -   Estate Planning - free will preparation -   Adoption Assistance -   Employee Assistance Program (EAP) -   MBTA Commuter & Transportation Subsidies (50% up to the federal maximum) -   Subsidized onsite parking, occasional parking, van pool, and car pool programs available -   Parents in a Pinch Back Up Child and Elder Care -   Credit Union -   Discounted Fitness and Gym memberships -   Pet Insurance -   Group Home & Auto Insurance -   Group Legal Program The Broad Institute is an equal opportunity employer. To learn more about the Broadís job opportunities, visit our Career Center at: <a href="https://www.broadinstitute.org/careers/career-center" rel="nofollow">https://www.broadinstitute.org/careers/career-center</a> If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=873362-1857-1539" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=873362-1857-1539</a>]]>

<![CDATA[ Development and enhancement of natural hazard models (tropical and extratropical cyclones,earthquakes, severe thunderstorm, etc.)<ul><li>Manage the collection and analysis of data; integrate the highest quality data into the modeling process</li><li>Perform validation and verification analysis of implemented model solutions</li></ul><ul><li><div> Ability to gather, understand, and critically analyze data from all relevant sources of natural hazard information</div></li><li>Solid technical programming skills gained through practical experience (e.g. C, C++, FORTRAN, Python,etc.), FORTRAN experience a big plus</li><li>Familiarity with manipulating large data sets, SQL experience a plus</li><li>Basic knowledge in statistics, familiarity with statistical packages such as R a plus</li><li>Highly motivated and self-directed with demonstrated experience in advancing complex projects</li><li>Excellent verbal communication skills</li><li>Risk modeling experience and/or GIS skills a plus</li></ul> Requirements: <ul><li>2+ years professional experience in a technical environment</li><li>MS degree in Physical Science or Engineering</li></ul> If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=873403-1857-5639" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=873403-1857-5639</a>]]>

<![CDATA[Project includes the design of improved pedestrian access on small (100ft by 50ft) site on the banks of the Charles River in Boston. Project includes: -Assistance with Wetlands Resource Area Delineation. -Preparation of Design Plans. -Preparation of a Notice of Intent to be filed with Boston Conservation Commission. -Preparation of Construction Documents. Please reply by e-mail ]]>

<![CDATA[Beckman Coulter develops, manufactures and markets products that simplify, automate and innovate complex biomedical testing. Our diagnostic systems are found in hospitals and other critical care settings around the world and produce information used by physicians to diagnose disease, make treatment decisions and monitor patients. Instruments for life science research are used by scientists as they study complex biological problems including the causes of disease, identify new therapies, and test new drugs. Our customers include hospitals, physicians´ offices, diagnostic reference laboratories, pharmaceutical and biotechnology companies, universities, medical schools and research institutions. In fact, Beckman Coulter has more than 200,000 clinical and research instrument systems operating in laboratories around the world. SNP - Applications Scientist This person will be the product specialist with the primary responsibility for the specialized Genomics Services offerings. In this capacity, the specialist will handle the development and production aspects of these projects within Genomic Services. Responsibilities will include project organization, coordination with production and R&D, completion of specialized techniques and final project data format. The specialist will be expected to review new technologies, develop process improvements and work with Manufacturing Services to implement improvements. Duties include: • project organization and data review • coordination with production and R&D • completion of specialized techniques • review of new technologies • development and implementation of process improvements Position Requirements: • BS/M.S. with 2+ years experience in molecular biology, biochemistry, chemistry, genetics or related field. Industry experience preferred. • Relevant molecular biology experience in a research laboratory, beyond standard course related laboratory work. • Strong communication skills with the ability to work in a multidisciplinary team environment. • Problem-solving and an ease with computers are a must. • Experience with sequence assembly and analysis software is a plus. If you believe your education and experience are in line with the position description and qualifications referred to above, and are motivated, energetic, and looking for a new and exciting opportunity, please submit your resume online at the URL below or at www.beckmancoulter.com. AN EQUAL OPPORTUNITY EMPLOYER - We believe that the mutual goals of our business and the community can best be met through our policy that consideration of race, color, religion, ancestry, national origin, sex, age, disability, veteran status or other protected characteristics, has no place in the selection, training or promotion of employees. In furtherance of this policy, we have developed a written Affirmative Action program to ensure positive action in providing equal opportunity for employees and applicants. ]]>

<![CDATA[Our client is seeking a talented and highly motivated candidate o join their Assay Development Group. Responsibilities: Using technology will develop quantitative In-Vitro Diagnostic immunoassays to meet regulatory requirements. Apply laboratory skills and experience in all phases of diagnostic product development from concept to commercialization. Requirements: BS/MS in Immunology, Biomedical Engineering, Biology, Biochemistry or related field with 3 - 10 years experience in diagnostic assay development Experience in all phases of immunoassay development including: applying DOE principles, preparing and executing test plans, adapting protocols and implementing appropriate statistical analysis Demonstrated productivity in a laboratory setting and excellent oral and written communication skills Excellent organizational, record keeping and communication skills Strong work ethic to generate high quality data under tight deadlines, collaborative and proactive attitude a must Must be US Citizen or Green Card Holder Please submit resume as word attachment to jobs@cwsciences.com Commonwealth Sciences, Inc. <a href="http://www.cwsciences.com" rel="nofollow">http://www.cwsciences.com</a>]]>

<![CDATA[Abcam, Inc., a rapidly growing company specializing in the production and sale of antibodies and related products, has a terrific opportunity for a highly motivated individual to get his or her foot in the door within the Biotech industry. Conveniently located in the heart of Kendall Square in Cambridge, MA, Abcam is currently seeking a Shipping Assistant to round out its team of dedicated and customer-focused logistics professionals. If you’re a recent graduate looking to launch your career or a more seasoned shipping/receiving professional seeking a position with genuine growth opportunities, look no further. At Abcam, hard work is rewarded and internal promotion strongly encouraged. Learn about our unique business and move your career forward in our interactive, fast-paced, and friendly environment! Shipping Assistant Responsibilities: • Ensure timely and accurate delivery of perishable products to end customers nationwide and to international Abcam locations  Select and package products; create waybills using our Abcam Order Management System.  Update status of orders and shipments in Operations Management System and track incoming shipments in Excel worksheet  Register, label, fill, and properly store product vials  Restock shipping supplies and fill ice freezers daily • Participate in continuous process improvement efforts by identifying areas for improved efficiency and customer service • Cross-train with Customer Service team to become acclimated with customer needs and order process. Assist with inbound phone calls as necessary. Qualifications: • Bachelor’s degree preferred (or in-progress) • Proficiency with MS Office applications (Excel, Word, PowerPoint, Outlook) • Meticulous attention to detail • Previous administrative/customer service experience, preferred In addition to a competitive salary, we offer an attractive flexible benefits package, which includes, profit-sharing, share options, generous vacation time, health/dental/vision/life/disability insurance and an outstanding 401k plan matching program. To apply, please use the following link to upload your resume and cover letter: <a href="http://www.abcam.com/index.html?pageconfig=careers&jobref=USTS009A" rel="nofollow">http://www.abcam.com/index.html?pageconfig=careers&jobref=USTS009A</a> Abcam, Inc. is a web-based business, with offices in Cambridge, UK, Cambridge, USA, Tokyo, Japan and Hong Kong. Our culture is one that empowers individuals, Visit our website, www.abcam.com, to learn more! Abcam Inc. is committed to diversity in the workplace. We seek to create an environment where all employees’ abilities and energies are fully utilized. We believe diversity enhances our opportunity to build a high-performance culture that enables us to succeed in a competitive business. ]]>

<![CDATA[The Howard Hughes Medical Institute conducts scientific research in leading medical and academic centers throughout the United States. We offer competitive salaries and an excellent, flexible benefits package that includes health, dental and vision insurance, generous personal time off, tuition reimbursement, and employer contributions to a 403(b) retirement program with immediate vesting We are looking for an energetic and highly organized research assistant interested in human genetics and cortical development. The position will involve assisting postdoctoral fellows and graduate students on molecular aspects of human genetics and related research. As a NIH and HHMI funded lab at Children’s Hospital Boston, our research is focused on the elucidation of fundamental mechanisms governing development of the human cerebral cortex. We use human genetics and animal models in conjunction with the latest molecular tools in our investigation of neuronal development. Requirements: • BA in biology or related field • Experience in working in a molecular biology lab • Good problem solving skills • Excellent organizational skills • Enjoy working as part of a team • We are looking for candidates who are able to make a 2 year commitment to the position. As a member of the research staff your duties and responsibilities would include: • Working with graduate students, postdoctoral fellows, and other staff members on research projects • Using and understanding a wide variety of molecular protocols including DNA sequencing, rtPCR, microsatellite analysis, and others • Data analysis • Extract DNA, RNA, and proteins from blood and tissue samples • Maintain equipment • Perform general lab maintenance Please email your cover letter and CV to R. Sean Hill Ph.D. at Jobs.WalshLab@gmail.com. ]]>

<![CDATA[Genstruct, a leading systems biology company in Cambridge, is seeking a senior software engineer to help build its next generation technology platform. The successful candidate will work as a member of our engineering team and be responsible for developing and refining our state-of-the-art knowledge repository, algorithm design and implementation, and collaborating with our scientists and modeling team to provide innovative solutions to systems biology problems. Requirements Candidates are expected to be able to operate independently, have a history of working with knowledge architectures and A/I, have excellent communication skills, be able to work as part of a fast-paced team, meet deadlines, have strong linear-logic based problem solving skills, and can effectively document and present ideas to others. Minimal Qualifications • authorized to work in the US without sponsorship • a Ph.D. in Computer Science or related discipline from a top-tier academic institution or 12+ years equivalent experience, • 5+ years experience in the design and implementation of knowledge representations (ontologies) and other artificial intelligence (AI) techniques, • 5+ years developing production quality code, preferably using Java and J2EE technologies, • 5+ years experience designing and implementing database storage solutions for knowledge-driven systems, • experience in Text Mining/NLP is strongly preferred, • a background in Graph Theory and Numerical Methods is required, • demonstrable experience of software engineering processes, particularly agile methodologies, source code management and issue tracking systems, • impeccable references, • a background in statistics or biology is a plus, • a background in Causal Modeling, Text Mining/NLP, and Agent Based Systems is also a plus. Submission Details • Email your resume and cover letter • Use "Senior Software Engineer" in the subject line to ensure delivery to the appropriate hiring manager • You MUST be authorized to work in the US without sponsorship • No relocation offered • NO Corp to Corp • NO recruiters, please About Genstruct Founded in 2002, Genstruct is a biotechnology company focused on elucidating the complexity of biology for the development of successful therapeutics. By modeling the components within the whole biological system, Genstruct delivers a deep molecular understanding of diseases and drug action, as well as mechanistic biomarkers to accelerate drug discovery and development programs. Genstruct engages in internal discovery and external development partnerships with top tier pharmaceutical companies, which apply systems biology in the areas of oncology, metabolic disorders, cardiovascular diseases and inflammation. The privately held company is based in Cambridge, Mass. For more information, please visit www.genstruct.com. ]]>

<![CDATA[Dana-Farber Cancer Institute is looking for a Research Technician to join their team! Candidates should have a firm understanding or prior experience with molecular biology techniques, including PCR, genotyping, cloning and tissue culture. Be able to work with rodents and organize large mouse breeding colonies. Job Qualifications BA, BS or higher degree. Schedule Full-time, 40 hours If interested please visit our website at: www.dana-farber.org and apply to req number 19572]]>

<![CDATA[We’re looking for a clinical research assistant for a full-time position at the Smoking Cessation Research Program through the Harvard School of Dental Medicine. This individual will work primarily on a study funded by the National Institutes of Health looking at the effect of extended duration counseling on smoking cessation. This is a great opportunity for those seeking clinical research experience to work with a principal investigator with 30+ years experience in the field of smoking cessation. The position requires the ability to both manage data effectively and to provide daily counseling in a therapeutic environment. Responsibilities include but are not limited to: - Conducting individual counseling sessions to provide participants with social support and skills training to quit smoking - Recruitment, enrollment and scheduling of participants - Management of large amounts of data and participant information - Grant proposal and manuscript preparation - General office management and ordering of supplies Qualifications: - Superior interpersonal and communication skills - Counseling experience preferred, although training will be provided - Excellent organizational skills and attention to detail - Self-motivated, independent worker - Ability to multitask and manage time effectively - Proficiency in Microsoft Office - Experience with SAS preferred - BA or Masters degree in Psychology preferred; those who intend to pursue a higher degree are encouraged to apply We are looking for a 2 year commitment with a start date of May 2010. If interested, please submit a resume, cover letter, and 3 references to the above address. ]]>

<![CDATA[The Division for Hematologic Malignancies is accepting applications for the position of Research Data Specialists to support the Hematopoietic Stem Cell Transplant (HSCT) Program at Dana-Farber Cancer Institute. The Research Data Specialist will support the HSCT clinical research program in the areas of data collection, computing, and database organization. Duties include the examination, synthesis, and evaluation of medical records; the abstraction and recording of pertinent medical information; and the monitoring of patient status. The Research Data Specialist will be responsible for the collection, management, and quality assurance review of patient clinical data. Job Qualifications Bachelor's Degree required. 0-2 years of related experience preferred. Computer skills, including proficiency in the use of Microsoft Office products, required. Requires close to moderate supervision. Experience working in a medical or scientific research setting or comparable technology orientated business environment preferred. Schedule Monday-Friday, 40 hours/week If interested please visit our website at: www.dana-farber.org and apply to req number 19530 ]]>

<![CDATA[Are you between the ages of 18-65? Brigham & Woman’s Hospital is looking for people who have been diagnosed with insomnia to participate in a research study. The study involves approximately 2 weeks of at home assessments and one 12 hour visit in our laboratory. Up to 4 screening visits may be required prior to beginning the study. Receive up to $300 at the completion of the study For more information please contact us (617) 732-6460 or email insomniastudy@partners.org ]]>

<![CDATA[ Participants needed for 9 Day Sleep Research Study on the effects of light on sleep at Brigham and Women's Hospital Do you fit these qualifications? *Must be 18-30 years old *Not on any medications *Non-smoker *Sleep about 8 hours/night THEN YOU MAY BE ELIGIBLE TO LIVE IN A LAB 24/7 FOR 9DAYS/NIGHTS! Receive up to $1,960 ** 3-5 week screening process, up to 5 outpatient visits before entering the study ** Contact Us at (617) 732-4311 ]]>

<![CDATA[Research assistant position available in Longwood Medical Area laboratory studying neurodegenerative diseases. Work focuses on both basic research aimed at understanding the molecular mechanisms of cell death in Alzheimer's and Parkinson's disease, as well as more translational efforts designed to identify therapeutic strategies in these disorders. Previous laboratory and histology experience helpful. Will consider both full and part time.]]>

<![CDATA[POSITION SUMMARY As Clinical Scientist, support the development of one or more oncology programs from pre-phase 1 through phase 3 and global registration. DUTIES & RESPONSIBILITIES Responsible for working collaboratively with the medical lead and team to execute the clinical program(s). Specific role will include some or all of the following responsibilities: Assist in planning, executing and reporting global clinical trials Conduct medical review of adverse events Assist in interpretation of efficacy and safety data from clinical trials Assist in ensuring regulatory compliance for clinical trials and reporting Assist in writing and designing standard protocols and amendments Assist in developing publications, abstracts, presentations, and/or clinical sections of regulatory documents. QUALIFICATIONS Basic qualifications: RN/Pharm.D. or equivalent (BA/BS/Ph.D. may be considered if the candidate has substantial oncology clinical research experience) 2-3 years oncology clinical research experience in an academic or in an industry setting Preferred qualifications: Proven scientific writing skills, with strong inter-personal, written/verbal communication skills Apply Link: <a href="http://bioemployment.jobamatic.com/a/jbb/job-details/198454" rel="nofollow">http://bioemployment.jobamatic.com/a/jbb/job-details/198454</a> ]]>

<![CDATA[Harvard FAS Center for Systems Biology A position is available for a post-doctoral fellow in an interdisciplinary research group that is developing and applying new metagenomic methods for analyzing the community structure, gene content, and transcriptional activity of the human gut microbiome. A major focus is on understanding how the microbiota and microbiome participate in the metabolism of various xenobiotics, including orally ingested drugs, and the impact of these activities on health, disease risk and therapeutic efficacy. Ideally, the candidate should have a PhD and research interests in comparative genomics, microbiology, computational biology, statistics, and/or biological chemistry/pharmacology. Applicants should send their CV, a 2-page statement of research experience and interests, and arrange for three letters of recommendation to be sent to Peter Turnbaugh, PhD, Harvard FAS Center for Systems Biology. Please reply to this posting with the necessary information. Harvard University is an Equal Opportunity/Affirmative Action employer.]]>

<![CDATA[RESEARCH TECHNICIAN: Dr. Jarrod Marto of the Dana-Farber Cancer Institute and Harvard Medical School seeks an exceptional research technician for his proteomics research group. This is intended as a temporary position, and is a particularly good opportunity for recent graduates who are seeking significant research experience prior to pursuing an advanced degree or medical school studies. The lab is focused on deciphering molecular mechanisms that underlie cell fate decision and other molecular hallmarks in human cancer. The incumbent will work closely with a senior lab member in a range of activities including: tissue culture, purification of protein complexes, purification of mRNA and qPCR, RNAi-mediated genetic manipulation, lentiviral propagation/infection, and flow cytometry. In addition to traditional low-throughput techniques, the laboratory is also building infrastructure and capabilities in high-throughput approaches for RNAi-mediated gene silencing as a functional readout for proteomics-based discovery experiments. The successful candidate for this position will be energetic, eager to learn new techniques, and excited by the opportunity to work in a supportive and collegial multidisciplinary lab environment. Additional requirements for this position include strong interpersonal and organizational skills, attention to detail, methodical record keeping, and a desire to contribute to research projects both independently and within a team. Minimum qualifications include a bachelor’s level degree in biomedical or related field, hands-on experience in laboratory research, and basic computer skills. Demonstrated experience in molecular or cell biology is preferred, but not required. The Dana-Farber Cancer Institute is a world-leader in clinical cancer care and basic research, and has committed significant, newly-renovated laboratory space for this research program. Interested candidates should email or send hardcopy of a cover letter and resume, including complete contact information for at least two references to: Dr. Jarrod Marto c/o Ms. Nicholle Wurie The Dana-Farber Cancer Institute 44 Binney Street, Sm 1158A Boston, MA 02115-6084 Email: nicholle_wurie@dfci.harvard.edu ]]>

<![CDATA[We're seeking an entry-level technician for some basic production tasks in a scientific manufacturing ernvironment. Duties include labelling bottles, dispensing powders, assembling test kits and basic documentation. Candidates are required to have a high school degree, excellent communication and documentation skills. Must live near the Chelmsford MA area and be reliable. Employment references will be required. Email resume to: jobs@cwsciences.com Commonwealth Sciences, Inc. <a href="http://www.cwsciences.com" rel="nofollow">http://www.cwsciences.com</a> ]]>

<![CDATA[A Boston-area consulting firm is looking for a junior-level candidate for an Environmental Safety & Health Technicians (ESH) position. The technician is responsible for supporting and maintaining compliance at a manufacturing site located in Southern Massachusetts. The position requires a working knowledge of EHS regulations and requirements (EPA, OSHA, DOT, etc.) and a familiarity with the ISO 14001 and OHSAS 18001 ESH management systems is preferred. The successful candidate should have good communication skills, both written and verbal, good presentation and training skills, excellent analytical and problem-solving skills, the ability to work independently and be a team-player. Other aspects of the position and our firm will be discussed with individuals selected for interviews. Candidates should submit their resume and a summary of their qualifications to the contact person below. Minimum requirements include a Bachelor’s degree in Health and Safety or Environmental or related technical discipline; 3 to 5 years of related work experience, and be located in or very near to Attleboro, MA. Compensation will depend on the candidates experience and qualifications. Send resume and letter to Aliana de la Guardia, Office Administrator at adelaguardia@theisogroup.com. Absolutely NO phone calls.]]>

<![CDATA[Adecco is looking for associates with 1-2 years experience in a lab or medical facility dealing with materials for a position as a material handler at a research facility in Andover. This is a great opportunity for recent college grads! A degree in the sciences is helpful but not required. 1-3 years experience working in a lab environment or medical facility.]]>

<![CDATA[The successful candidate will perform biological and biochemical experiments aimed at the study of dengue virus biology and characterization of candidate anti-dengue virus inhibitors. This includes in vitro tissue culture experiments as well as experiments performed in murine models of virus infection/replication and pathogenesis. Laboratory techniques will include plasmid preps, PCR, real-time PCR (QPCR) and real-time RT-PCR (qRT-PCR), cloning; Southern, Northern, Western blot; immunoprecipitation; immunofluorescent staining, fluorescence microscopy; cell culture, and viral plaque assays. Initially, the candidate will be responsible for assisting current lab members with their projects and will also be responsible for helping with general lab tasks and maintenance. As the successful candidate demonstrates proficiency and efficiency in the lab, opportunities to work more independently will be available. The successful candidate will also perform related duties as required. A willingness to learn and a keen interest in experimental science are essential. This is a one-year grant funded position. Basic Qualifications: College background or equivalent work experience in experimental science; 1-2 years related work experience (relevant coursework may count towards experience). Additional Qualifications: Undergraduate degree in biology or 2 or more years in an academic research setting; prior experience in a research laboratory; comfort working with and around BL2 viruses, including dengue virus, hepatitis B, hepatitis C, poliovirus; prior experience with standard molecular biology and cell biology is preferred; tissue culture experience, virology experience and experience working with rodent models is preferred, but a willingness to learn these techniques is an acceptable substitute. Pre-Employment Screening: Identity All applicants must apply via our website (please see requistion number 20468BR): <a href="https://sjobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?SID=" rel="nofollow">https://sjobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?SID=</a>^hP_slp_rhc_3d0vgYRNz29LaRoXAQMVcMo_slp_rhc_PPvHza7RRTkc_slp_rhc_2pT2yjs8VbysMrE9UtQBGPlaerFQxUOg787X_C_R__L_F_muxnhRcNSXLFCoC9PGc13Lh/Xc0n5H4=&jobId=577365&type=search&JobReqLang=1&recordstart=1&JobSiteId=5341&JobSiteInfo=577365_5341&GQId=0 Applicants can also go to our employment website: www.employment.harvard.edu and apply directly to requisition 20468BR. Harvard is an Affirmative Action/Equal Opportunity Employer ]]>

<![CDATA[Eastern Cooperative Oncology Group/Frontier Science ECOG (www.ecog.org) is one of the largest clinical cancer research organizations in the United States, and conducts clinical trials in all types of adult cancers. ECOG’s network includes nearly 6000 physicians, nurses, pharmacists, statisticians, and clinical research associates (CRAs) from the U.S., Canada, and several other countries worldwide. We work toward the common goal of controlling, effectively treating, and, ultimately, curing cancer. Frontier Science (www.fstrf.org), the grantee, is a non-profit foundation and offers excellent working conditions and outstanding benefits, including 4 weeks’ paid vacation. Position Summary: The Data Associate acts as a liaison between the ECOG Coordinating Center and our multiple contacts including nurses and doctors in hospitals and clinics all over the US and internationally. These institutions enroll patients on our clinical trials. Their patient data is submitted to the Coordinating Center on ECOG specific case report forms. This data is carefully reviewed by the Data Associate to ensure it is reported in a timely and accurate way, and in adherence to the trial. The Data Associate is responsible for managing the data on one large or multiple small trials, typically focused on one particular disease site (ex. gastrointestinal or brain cancer). Duties Include: Assists with the data management of assigned clinical trial(s)/project(s): quality control and evaluation of clinical patient data; preparation of data for computer entry; write data queries/data clarification forms (DCFs) to institutions and resolves DCF’s in database when returned by institutions; ensure that toxicity, response, follow-up, and survival data are accurately coded and updated in the database; review and provide input for protocols and addenda in development. Also may be required to provide input in the development of case report forms and associated submission schedule, study parameters, and patient eligibility checklists. Assists the study chair and statistician to prepare database for analysis. Serves as a back up for the randomization staff in registering patients and drug ordering team members. May be required to perform and trouble shoot all randomizations, manual and electronic. Other duties as assigned. Travel to our bi-annual group meeting may be required. BA/BS preferred, experience will be considered. Full Time, 40 hour position, Monday – Friday during normal business hours (8-4 or 9-5). Our office is located close to several public transportation routes, including the Green Line B train, the route 57 bus from Allston and Watertown, and the CT2 cross-town bus route between Cambridge and Ruggles station. How to Apply: Please submit cover letter (job code DACL) and resume to resumes@jimmy.harvard.edu. Resumes submitted without a cover letter will not be considered. Please include preferred salary range. Frontier Science is a participant in the federal E-Verify® program EOE/AA ]]>

<![CDATA[Chronic Pain Research – CRO Small, fast growing company located in Natick with a new Clinical Research Center looking for a candidate to build this center and a specialty CRO from the ground up. Searching for a Director of Clinical Operations who can: hire and build their team, organize the logistical operations of the center, meet all regulatory needs, help write standard operating procedures, and shepherd the conduct of our clinical trials. The right candidate will be able to function completely independently. Responsible for everything including Protocol Development, Investigators, CRA oversight, study management, project management, budgets, etc. This candidate must have a can do attitude, be resourceful, and have a high level of responsibility. If you have significant experience and a history of excellent performance, please e-mail your resume and salary expectations to HR@analgesicsolutions.com. Salary DOE ]]>

<![CDATA[. Paratek Pharmaceuticals is small biotech company of approximately 40 employees and we are located at 75 Kneeland Street in Boston. We currently have an exciting novel antibiotic compound in Phase 3 trials and need additional clinical research coordinator support. This position offers a fast-passed, collaborative environment where there is a high potential for a motivated individual to increase their clinical research skills very quickly. Requirements of all applicants: 1. Bachelor Degree (in science related field a plus) 2. At least 6 months of prior work experience as a Clinical Research Coordinator 3. Proficiency with Microsoft Office applications 4. Positive attitude, detail orientated and self-motivated Position Description 1. Attend and participate in various internal and external meetings, including Clinical Operations Team meetings, vendor selection meetings, vendor kick-off meetings, and investigator meetings. 2. Work with the clinical sites all ongoing phase 1-3 studies. 3. Coordinate and manage the review and tracking of documents for multiple Clinical studies, including clinical “essential" documents, contracts, and financial records. 4. Receive and review documents according to ICH and GCP guidelines; prioritize document review to meet agreed deliverables and timelines. 5. Assist clinical team members with filing paper and electronic documents; Scan and import documents into an electronic filing system. 6. Review documents according to Regulatory requirements prior to obtaining approval for drug release. 7. Communicate with outside vendors regarding document issues/discrepancies. 8. Maintain the Clinical Intralinks document repository with partner Novartis. 9. Become proficient in using our EDC system and generate reports when requested. 10. Assist in coordinating internal and external meetings as well as taking detailed minutes from those meetings. 11. Maintain security and confidentiality of documents. ]]>

<![CDATA[Are you interested in participating in a clinical research study for Low Back Pain? Diabetes? please contact us at 508-584-2030. Compensation for time & travel provided Some other studies Beacon Clinical Research is currently recruiting patients to participate in are, COPD Diabetes (type I & II) Diabetic Painful Neuropathy Gerd (acid reflux) High Blood Pressure High Cholesterol Hypertension Lower Back Pain Osteoarthritis Osteoporosis Ulcerative Colitis If you are interested please contact Beacon Clinical Research at 508-584-2030 or visit them on the web at www.beaconclinical.com Compensation for time & travel is provided to you ]]>

<![CDATA[We are looking for enthusiastic, motivated and hard working individuals to fill several entry level Pharmacy Technician Assistant positions. No previous experience is required and we provide on the job training to guide you along a career path that can allow you to become a Pharmacy Technician. Responsibilities include: • Ensuring all procedures are performed in compliance with company policies; • Logging use, maintenance and cleaning of equipment; • Labeling products according to company standards; • Ability to successfully communicate and interact with other employees. Skills Required: • Able to perform simple and complex mathematical problems; • Focus and attention to detail; • Excellent communications skills; • Ability to multi-task in a fast-paced environment; • Ability to work independently; • Team-player. Personal Attributes • Have accurate visual discrimination skills; • Able to perform repetitive work movements/manipulations; • Able to work in a fast-paced environment; • Able to stand for long periods of time. Must have at least a High School Diploma/GED and a command of the English Language. Must be available to work Full Time. Must be flexible to work a shift between 6AM and 8PM. Interested candidates should submit their resume, along with salary requirements, to (508) 475-0556 or hr@medicalsalesmgmt.com ]]>

<![CDATA[Instrumentation Laboratory is the main company of a major multinational group, a world leader in the development of in vitro diagnostic reagents and instrumentation. Since its founding in 1959, IL has led the rapidly evolving markets of clinical diagnostic systems for blood gas/electrolytes analysis, hemostasis and clinical chemistry. IL’s renowned medical technology is used every day in thousands of hospitals and laboratories around the globe. It is IL’s focus on its customers-and on the patients whose lives are touched by its products-that is guiding the company into the next century. Senior QC Analyst Position Summary Performs analyses using various automated and manual methods in accordance with established Quality standards and GMP requirements. Principal Duties & Responsibilities: - Statistical Analysis of process and experimental data - Set up, define and monitor an SPC program for testing analytical test data - Analysis of process capability (Cpk/Ppk) related to in-process testing, incoming supplier AQL data and new product configurations - Data analysis of test fixtures to determine module reliability, performance and bias - Monitor production processes for correlations between yield and components, parts or assemblies Minimum Skills & Knowledge Requirements: A B.S./B.A. Degree in mathematics, statistics, chemistry or applied science or engineering is required. Strong knowledge of production statistics Working knowledge of MSAccess, MS Excel and Minitab Lean-Six Sigma training strongly preferred. If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Instrumentation Laboratory appreciates and values diversity. We are an Equal Opportunity Employer M/F/D/V Please use the following link to apply: <a href="http://www.instrumentationlaboratory.com/sitecore/content/ilus/Careers/Job%20Opportunities.aspx?action=viewDetails&accountId=44679f85e2332fe1ab781f5d20a065e96d2851e1&jobId=0637&jobSource=Craigslist" rel="nofollow">http://www.instrumentationlaboratory.com/sitecore/content/ilus/Careers/Job%20Opportunities.aspx?action=viewDetails&accountId=44679f85e2332fe1ab781f5d20a065e96d2851e1&jobId=0637&jobSource=Craigslist</a> OR www.ilus.com]]>

<![CDATA[Instrumentation Laboratory is a major multinational company, a world leader in the development of in vitro diagnostic reagents and instrumentation. Since its founding in 1959, IL has led the rapidly evolving markets of clinical diagnostic systems for blood gas/electrolytes analysis, hemostasis and clinical chemistry. IL’s renowned medical technology is used every day in hundreds of hospitals and laboratories around the globe. It is IL’s focus on its customers-and on the patients whose lives are touched by its products-that is guiding the company into the next century. Senior Process Engineer Position Summary: Chemical Engineering/Chemistry resource to provide process development, troubleshooting, and ongoing support for GEM sensor card manufacturing. The successful candidate should have a proved track record of developing and implementing process improvements related to sensor design in a regulated medical manufacturing environment. Principal Duties & Responsibilities: • Lead process improvement projects. Perform project management, planning, scheduling, and resource allocation. • Provide hands-on problem solving support to manufacturing. Analyze test results and process yields to identify and prioritize improvement opportunities. • Design experiments, analyze internal and customer data to identify and solve problems. • Write validation plans, experimental plans and reports, equipment specifications, etc. • Write change orders to improve quality, costs, documentation, and/or regulatory compliance. • Research technologies and techniques for applicability to current and future products. • Must be independent top-level technical resource as well as team player. Minimum Skills & Knowledge Requirements: • Requires a B.S. in Chemical or Biomedical Engineering or Chemistry, MS preferred. • Five years experience in the manufacture and/or development of complex processes or products. • Must possess broad technical knowledge in engineering and chemistry as well as other applicable technologies. • Direct experience working in FDA cGMP and ISO 13485:2003 regulated manufacturing environments. • Experience in technical support within medical device manufacturing. • Six Sigma experience; Green Belt minimum is preferred • Strong technical writing background with a solid statistics knowledge base related to medical device process validations. • Experience with data analysis software used to extract and analyze data, MS Access, Excel and Minitab preferred. If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your application. Instrumentation Laboratory appreciates and values diversity. We are an equal opportunity employer. M/F/D/V. Please use the following link to apply: <a href="http://www.instrumentationlaboratory.com/sitecore/content/ilus/Careers/Job%20Opportunities.aspx?action=viewDetails&accountId=44679f85e2332fe1ab781f5d20a065e96d2851e1&jobId=OPS-09-33&jobSource=Craigslist" rel="nofollow">http://www.instrumentationlaboratory.com/sitecore/content/ilus/Careers/Job%20Opportunities.aspx?action=viewDetails&accountId=44679f85e2332fe1ab781f5d20a065e96d2851e1&jobId=OPS-09-33&jobSource=Craigslist</a>]]>

<![CDATA[We are looking for a QC Chemist to perform chemical testing of raw materials, intermediates, and Active Pharmaceutical Ingredients (API’s) in support of process research, discovery research, cGMP production, and stability testing. ESSENTIAL FUNCTIONS / PRINCIPAL ACCOUNTABILITIES: The chemist works independently on most analyses, with direction on more complicated analyses, methods development, and project management. The chemist is expected to: * Learn analysis techniques and applies learning to standardized methods * Apply basic scientific knowledge to solve simple analytical problems * Learn and follow all SOPs and GMPs * Conduct analyses and interprets results. * Transfer and modify analytical methods with guidance. * Prepare documentation in accordance with SOPs. * Review other team members analytical data for simple tests. * Calibrate instruments and contribute to laboratory organization and compliance. * Perform testing for the qualification of reference standards EDUCATION REQUIRED (DEGREE / MAJOR / CERTIFICATIONS): * Requires a minimum of a B.S in chemistry or closely related discipline and 0-3 years of experience, or extensive experience in the analytical chemistry or pharmaceutical QC fields. Prior experience with HPLC and GMP required. ]]>

<![CDATA[An Associate Scientist (Level II) will work in the Research Biology Department at the ALS-Therapy Development Institute in Cambridge, MA to support in vivo and in vitro validation of candidate therapeutics in murine models of Amyotrophic lateral sclerosis (ALS). This candidate will be responsible for the following three jobs: 1. Weekly genotyping of transgenic mice using an in-house, automated Q-PCR platform. 2. Support and development of enzyme linked immunosorbent assays (ELISA) for weekly, large-scale pharmacokinetic studies. 3. Development of assays for protein characterization such as immunoblots, immunoprecipitation, and immunohistochemistry. The candidate will work closely with internal in vitro and in vivo research teams, as well as external vendors, to support ongoing preclinical studies in a mouse model of ALS. Academic Qualifications and Technical skills: The candidate must have a BS or MS in biology, biochemistry, or molecular biology and 3+ years of experience in molecular biology techniques including nucleic acid purification, PCR, Q-PCR, ELISA, and immunoblotting. Working knowledge of spreadsheet programs, is also required. Ideally, the candidate will have experience with molecular biology automation. Strong communication skills and a team orientation are essential. The Amyotrophic Lateral Sclerosis Therapy Development Institute (ALS-TDI) is a non profit biotech focused on the discovery and development of therapeutics to treat ALS. The institute is a world leader in the pharmacological testing of lead candidates in animal models of ALS and has established expertise in the utilization of genomics and proteomics technologies for drug discovery. Please submit resume and cover letter. ]]>

<![CDATA[Biotech Patent Assistant Full time, ENTRY LEVEL technical assistant position. Seeking motivated individual with a four year degree in biology, biochemistry, chemistry, or the like to assist biotech and chemical patent attorneys with various aspects of their patent prosecution and opinion practices. Excellent reading, writing, communication, computer and organizational skills are imperative. Must be able to work independently, as well as with others, to meet strict client project deadlines often under short time constraints. Strict attention to detail is mandatory. 1 – 2+ years business experience preferred. Law firm or in house patent experience a plus. Will train the right individual. Location: Portsmouth, NH Compensation: $30k starting salary, health, dental, vision, disability, life, 401k, tuition reimbursement, and profit sharing. Please forward your cover letter and resume to Careers@seqidno.com. No phone calls please. ]]>

<![CDATA[TECHNICAL ASSISTANT MIT Department of Biological Engineering The Department of Biological Engineering at the Massachusetts Institute of Technology (MIT) seeks a technical assistant to assist lab members in computational analysis of Illumina sequencing results including ChIP-Seq and mRNA-Seq data. Will also benchmark alternative methods for analyzing data and developing user-friendly interfaces for algorithms developed in the lab. Requirements: a bachelor's degree in computer science or related area; demonstrated skill analyzing biological data; ability to work well in a team setting; and strong programming skills, including knowledge of Python and MATLAB. Experience in analysis of ChIP-Seq or alternative splicing data desirable. Interested candidates may apply on-line at <a href="http://web.mit.edu/jobs" rel="nofollow">http://web.mit.edu/jobs</a> Please reference job number mit-00006805 and indicate where you saw this web posting. MIT is an equal opportunity/affirmative action employer. Applications from women, minorities, veterans, older workers, and individuals with disabilities are strongly encouraged.]]>

<![CDATA[A loving and welcoming Weston household is seeking an Academically-Oriented Personal Assistant. Major job responsibilities include participating in managing demanding school academics and activities for two academically strong girls, tutoring, managing a busy, happy and complex household, coordinating schedules and transportation for the girls, and serving as an administrator for household business. This is an excellent position for a middle or high school teacher or a loving professional looking for a change from a traditional office setting. The successful applicant is warm, flexible, responsible, enjoys the highest ethical standards, self-motivated, kind, of calm self-confident demeanor, and capable of multi-tasking and keeping up with the intense, frequently changing schedule of this busy family. This is a full-time professional position with excellent benefits. Schedule includes evening work several days a week. Duties will include (but are not limited to): - overseeing children’s academics at a high quality level - tutor in middle and high school subjects - driving children to and from school/activities - event and entertainment planning - travel planning - shopping and running errands - filing - correspondence - answering phone - packing - laundry - optional night/weekend babysitting The candidate needs to love children and dogs. Other attributes of a successful candidate: - positive “whatever it takes” attitude - self-motivated - reliable and flexible - highly intelligent - strong educational background; a Masters degree is preferred - a Math or Science background is a plus - extremely organized - ability to work fast and effectively multi-task - computer skills (internet, e-mail, scheduling, use of expense software) - excellent references - looking for a long term commitment on both sides - drivers license and safe, reliable car - good communication skills (perfect English) - proof of ability to work in US This is a unique, FUN, challenging and rewarding position. Please send resume and contact information to confidential email address. ]]>

<![CDATA[Clinivation- the industry leader in Enterprise Market Clearance Solutions- seeks senior, experienced, and entry-level Regulatory Affairs Specialists to lead, manage, and contribute to important professional services engagements for global medical device and diagnostics companies. Clinivation’s market clearance solutions are used by more than 100 medtech industry leaders- Johnson & Johnson, St. Jude Medical, Smiths Medical, Terumo, Philips, etc.- to create new international revenue by accelerating the worldwide commercialization of their medical products. Our engagements are strategic, high-impact, and have a global scope. The successful applicant will be a mature, intelligent, and motivated professional. RESPONSIBILITIES: -Manage and contribute to important client engagements. Your assignments and roles will be appropriately matched to your skills and experience. -Leverage biomedical and technical expertise, technical writing abilities, and management skills to successfully deliver market clearance solutions into a broad range of industry engagements. -Effectively report and function internally, deliver accurate project reports, and maintain enterprise content management systems. -Travel (US and international) of ~ 0 - 20%. -Will consider full-time, part-time, contract-to-permanent, and contract MUST REQUIREMENTS: -Polished and mature writing, communication, and technical skills to represent clinivation's domain expertise and leading technologies to customer senior business and regulatory executives. -Strong technical writing skills. -Undergraduate degree- with academic success- plus professional training. PREFERRED REQUIREMENTS: -3+ years of successful biomedical industry regulatory, clinical, and/or quality experience; and 5+ total years industry experience. -Medical device or diagnostics industry vertical experience -Graduate technical degree in biomedical engineering, life sciences, and/or related fields. -Professional certifications and/or licensures. APPLY: Apply online, submit your resume to recruiting@clinivation.com , or fax to 508-655-6561. ]]>

<![CDATA[Clinivation- the industry leader in Enterprise Market Clearance Solutions- seeks senior, experienced, and entry-level Regulatory Affairs Specialists to lead, manage, and contribute to important professional services engagements for global medical device and diagnostics companies. Clinivation’s market clearance solutions are used by more than 100 medtech industry leaders- Johnson & Johnson, Siemens, Smiths Medical, Terumo, Philips, etc.- to create new international revenue by accelerating the worldwide commercialization of their medical products. Our engagements are strategic, high-impact, and have a global scope. The successful applicant will be a mature, intelligent, and motivated professional. RESPONSIBILITIES: -Lead, manage, and contribute to important client engagements. Your assignments and roles will be appropriately matched to your skills and experience. -Leverage biomedical and technical expertise, regulatory affairs knowledge, and management skills to successfully deliver market clearance solutions into a broad range of industry engagements. -Work with our professional services and software teams to translate customer requirements into successful solutions. -Effectively report and function internally, deliver accurate project reports, and maintain enterprise content management systems. -Travel (US and international) of ~ 10 - 30%. MUST REQUIREMENTS: -Polished and mature communication and technical skills to represent clinivation's domain expertise and leading technologies to customer senior business and regulatory executives. -Strong analytic skills and acumen. -Technical degree- with academic success- plus professional training. PREFERRED REQUIREMENTS: -3+ years of successful biomedical industry regulatory and/or quality experience; and 5+ total years industry experience. -Medical device or diagnostics industry vertical experience -Graduate technical degree in biomedical engineering, life sciences, and/or law. -Professional certifications and/or licensures. APPLY: Apply online, submit your resume to recruiting@clinivation.com , or fax to 508-655-6561. ]]>

<![CDATA[OVERALL RESPONSIBILITY This is a 6 month temporary position. Performs comprehensive annotation and analysis responsibilities to advance the objectives of the Microbial Sequencing Center utilizing bioinformatics tools as computational techniques, under the direction of the Manager, Genome Annotation. CHARACTERISTIC DUTIES - Annotates finished chromosomes in mammalian, fungal and bacterial genomes using bioinformatics and computational techniques and concepts. - Utilizes various computation analyses and biological interpretation of results to review existing annotations and propose improvements. - Performs manual annotation on mammalian, fungal and bacterial genomes and interprets results from similarity searches and gene finding programs. - Runs and validates genome annotation pipeline; ensures that all annotation objectives are met as required by the project. - Tests bioinformatics annotation and analysis tools developed in-house and provides feedback to the software development team. - Performs other related responsibilities as necessitated by the position or as assigned by the Manager. QUALIFICATIONS - Master’s degree in bioinformatics or related field, or BS with substantial related experience - Demonstrated knowledge of bioinformatics concepts, methods, and tools - Experience working in SQL, Oracle, and Perl or Jython - Familiarity with genomic data, tools and databases - Strong attention-to-detail and analytical skills - Ability to work effectively in a team environment The Broad Institute was launched to pioneer a new model of collaborative biomedical science that would transform medicine. To accomplish these goals, we have built an amazing team of talented Broadies who work together to realize this transformation. The Broad Institute is an equal opportunity employer. To learn more about the Broad’s job opportunities, visit our Career Center at: <a href="https://www.broadinstitute.org/careers/career-center" rel="nofollow">https://www.broadinstitute.org/careers/career-center</a> If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=869732-1857-2139" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=869732-1857-2139</a> ]]>

<![CDATA[Commonwealth Sciences, Inc. is a Boston area recruiting firm specializing in life sciences and engineering. We work with scientific and engineering professionals at a variety of levels and disciplines primarily in the Biotechnology, Pharmaceutical, Medical Device and Clinical Research industries. We are currently seeking an experienced recruiter / account manager to join our growing business. Responsibilities include developing new business with pharmaceutical, biotech, diagnostics and medical device companies through inside and outside sales activities including lead generation, cold calling, networking and marketing campaigns. Duties also include sourcing and recruiting science candidates through the internet, networking events, call marketing, job fairs and campus recruiting. Commonwealth Sciences offers an ethical and entrepreneurial atmosphere where your independence, creativity and drive can develop and flourish. We invest heavily in the latest recruiting tools and technology to optimize your ability to compete and succeed in a competitive market place. We also offer one of the most lucrative commission plans in the business. Qualifications must include a Bachelors Degree in a technology or business discipline with outstanding communication and interpersonal skills. Experience in sales and/or recruiting in a high-tech environment or the staffing industry with a stable and proven track record is essential. A life science or engineering background is preferred. Candidates must have a strong drive and work ethic with the ability to operate independently in a fast paced environment. Local candidates are highly preferred. Email you resume to: jobs@cwsciences.com Commonwealth Sciences, Inc. <a href="http://www.cwsciences.com" rel="nofollow">http://www.cwsciences.com</a> ]]>

<![CDATA[We have a Contract opportunity with a prominent client for a Scientist in Cambridge, MA. Experience in mammalian cell culture, generation of stable cell lines, transient transfection of cell lines and FACS. •Proficient in genetic screening with siRNA/shRNA/cDNA by conventional or viral transduction technologies. •Experience with various protein technologies including, but not limited to Western blotting and immunoprecipitation. •Solid molecular biology experience including qPCR, site-directed mutagenesis, and DNA cloning. •Experience with Biacore technology and ELISA development a plus. •Excellent communication and presentation skills BS or MS in Biochemistry, Molecular Biology, Cell Biology, with 3+ years of laboratory research experience. For immediate consideration, please forward a current copy of your Word formatted resume to jason@thefountaingroup.com. ***Due to the volume of responses received, only qualified candidates will be contacted but your resume will be filed for future openings***]]>

<![CDATA[We have an immediate need for a Temporary Quality Assurance Associate to work through the end of March. Duties and responsibilities •Review batch records for product release; identify errors, omissions, and deviations and reconcile or correct. •Review and accept incoming raw materials. •Participate in additional compliance related programs to support ISO-9001 Quality Management System. Qualifications/Requirements •Previous experience related to protein manufacturing. Knowledge of fermentation, downstream processing and purification of proteins preferred. •Knowledge of ISO-9001 Quality Management Systems including Corrective Action / Preventive Action, deviation and change control programs preferred. •Bachelor’s degree in biology or chemistry plus 2-3 years in biologics manufacturing and/or quality assurance. Knowledge of protein purification and fermentation a plus. Please send resume in either MS Word or PDF format to: resumes@repligen.com ]]>

<![CDATA[Beth Israel Deaconess Medical Center, a teaching hospital of Harvard Medical School, is renowned for excellence in patient care, biomedical research, teaching and community service. Located in the heart of Boston's Longwood Medical and Academic Area, it hosts nearly three quarters of a million patient visits annually in and around Boston. The Division of Vaccine is dedicated to studying all aspects of HIV pathogenesis and vaccine development. We are currently seeking a research assistant to participate in our ongoing efforts to study HIV immunology and to develop a safe and effective vaccine for HIV. We currently have active research programs in the construction of novel vaccine vectors, preclinical studies, and phase I clinical trials. Responsibilities will include laboratory-based assessments of candidate vaccines in preclinical models, processing samples from clinical trials, immunologic assays, vector development, molecular biology, and tissue culture. Bachelor's Degree Required. Prior experience with flow cytometry and/or cellular immunology would be desired. We offer a competitive compensation/benefits package with a generous earned-time program, 401(k)/403(b), subsidized T-pass program, health and fitness facility, and more! Equal Opportunity Employer. To apply, please visit our website at www.bidmc.org and apply for requisition number 10-0427. ]]>

<![CDATA[Participants needed for 9 Day Sleep Research Study on the effects of light on sleep at Brigham and Women's Hospital Do you fit these qualifications? *Must be 18-30 years old *Not on any medications *Non-smoker *Sleep about 8 hours/night THEN YOU MAY BE ELIGIBLE TO LIVE IN A LAB 24/7 FOR 9DAYS/NIGHTS! Receive up to $1,960 ** 3-5 week screening process, up to 5 outpatient visits before entering the study ** Contact Us at (617) 732-4311 ]]>

<![CDATA[Gnarus Advisors LLC seeks a library sciences-trained individual to design and maintain a specialized library for environmental sciences. This library is a combination of hard- and electronic-copies of project documents and open literature on topics of waste management and their regulation in general and for specific industries (e.g., mining, plastics, etc.). Qualifications: The selected candidate will have the following capabilities: • Storage and retrieval system design, including appropriate software; • Cataloguing; • Information searches, including in-house, outside library, internet, client databases, etc. • Project document management (some projects have thousands of documents); and • Tracking topics of interest for technical staff. Demonstrated training and/or experience with the above capabilities is required. The position is 30-40 hrs/wk, including an excellent benefits package.]]>

<![CDATA[ This position requires someone with excellent communication and organizational skills. Attention to detail is a must. We are looking for someone who is able to deliver high productivity while maintaining high quality standards. This position is for someone who will be working as a research assistant to a Harvard Assistant Professor in a Neurology Clinical Research Laboratory. This individual will be responsible but not limited to: - Excellent interpersonal and management skills with facility to interact professionally at all levels and plan and initiate new activities. - Ability to compile and manage data, analyze information, and produce reports. - Administrative skills to meet the regulatory compliance required by IRB reporting. - Excellent written and verbal communication skills. - High level time management skills requiring exceptional organizational skills and the ability to organize time and prioritize effectively. This includes the ability to ask for direction when appropriate and the flexibility to handle multiple tasks and deadline pressures. - Experience with common PC computer software including Microsoft Word, PowerPoint, Excel, Access and Outlook, and reference management software such as Reference Manager or EndNote. - Facility with learning new computer applications. - Perform literature searches using PubMed and other search engines, and perform Internet searches using MS Internet Explorer and various search engines. - Typing speed of 50+ wpm. - Superb proofreading skills. - Ability and willingness to learn new research and administrative skills. - Ability to conduct reference and literature searches. - Ability to compile and manage data, analyze information, and produce reports. - Assist with materials management, supply, inventory, and ordering of program materials. - Knowledge of current and developing trends in areas of professional expertise. The interested candidates should be aware that this is a job in an extremely busy environment and therefore with a high volume of work and responsibility. We are looking for candidates who can meet the demands of this job. If you are interested, please send us your CV and cover letter for screening to official application. ]]>

<![CDATA[Several full time research positions are available at the Massachusetts General Hospital for graduating seniors interested in spending a year or two before continuing their education in medical or graduate school, as well as for individuals with somewhat more experience, including students with Masters Degrees. Previous holders of this type of position have had the opportunity to work on research projects and to publish scientific papers on their work, and many individuals have published first-authored papers on their work. For students with an interest in medicine, exposure to clinical medicine is encouraged. The work of our group has concerned: the assembly of data, and the development of improved mathematical methods, for predicting the outcome for cancer patients; the identification of screening schedules for reaching the maximal possible reduction in cancer death achievable by cancer screening; the application of modern computer speech and telephony for developing scheduling/reminder systems for increasing the use of preventative medical interventions such as mammography and influenza immunization. The program is a collaborative project between individuals at the Massachusetts General Hospital, Harvard, and MIT, and is located in an MGH facility next to MIT in Cambridge. These positions are available as of June 1. But students who wish to begin working part time in the spring semester are encouraged to do so. The first position concerns the assembly and analysis of data on cancer and its outcome. An interest in medicine, and a familiarity with the use of Excel and Access is essential. The candidate need not have a strong background in mathematics or computer science, although this would be desirable. The second position concerns the analysis of the systems that hospitals use to make medical appointments, with the aim of improving utilization of preventive service such as cancer screening. This position also concerns managing preventive health interventions that use these systems. The third position concerns the refinement, implementation, and testing of a system that sends computer generated telephone reminder messages for increasing the use of breast cancer screening. Knowledge of, or ability to learn, ASP, ASP.net, AJAX, C#, HTML, MS SQL Server, Windows Server 2003 security, and general database and server administration is required. Skill with VXML and computer speech would also be desirable. The fourth position concerns the development of improved mathematical methods for predicting cancer outcome. Related work concerns the development and implementation of novel mathematical methods for Web-based calculators that physicians can use for predicting the risk of cancer recurrence, as well as the development of computer simulation models of cancer progression. The fifth position concerns the creation of telephone reminder scripts, which our systems will launch to recruit patients to schedule appointments for cancer screening. This position would be suitable for a person with interests in advertising, copywriting, English, marketing, social marketing, persuasion psychology, health communication and public health. This position also concerns managing preventive health interventions that use these scripts. Reply by email with CV or resume to: James S. Michaelson Ph.D. Department of Pathology Harvard Medical School & Departments of Pathology and Surgery Massachusetts General Hospital ]]>

<![CDATA[About Genstruct Genstruct is a successful, growing, socially conscious and highly intellectual company with a highly collaborative working environment. Over 70% of our staff hold PhD or MD degrees. Our work environment is open, friendly, and high energy. Our company offers excellent benefits, flexible working arrangements, and numerous opportunities for professional growth. Genstruct works collaboratively with leading pharmaceutical and consumer products companies to use Systems Biology to advance their research and development programs. Genstruct is also independently developing efforts in personalized medicine and systems toxicology that leverage the Genstruct Technology Platform. Our team consists of scientists, engineers, statisticians, project managers and business leaders, all focused on the integration of systems biology into mainstream biotechnology and pharmaceutical product development. Genstruct is headquartered in Cambridge MA, near the Alewife T station. About this Position Genstruct needs an experienced Scientific Project Manager to internally manage and support collaborative scientific projects with biotech, pharmaceutical, and consumer product partners. This position supports multiple scientific project teams simultaneously. Candidate must be highly organized, flexible, and adept at handling multiple projects and tight deadlines. Track record of success in project management is essential, as is the ability to communicate the progress of projects and conclusions to senior management in a concise, clear manner. Formal project management training and experience in molecular or cell biology are desired. Key Responsibilities • Ensures quality execution of project work plans and revises as appropriate to meet changing needs and requirements • Identifies and monitors project resources needed to achieve project goals • Creates timelines and lists of responsibilities and works with project lead to ensure adherence • Works with scientific project lead to coordinate day-to-day operational aspects of a project • Plays key role in quality control and quality assurance by reviewing all deliverables prepared by team before delivering to client including Word documents and PowerPoint presentations • Ensures project documents are complete, current, and stored appropriately • Works closely with scientific consulting team to quickly resolve issues and keeping projects on track • Identifies potential project challenges before they arise and preemptively identifies possible solutions • Communicates effectively within all areas of Genstruct (this position will initially be largely internal-facing) • Effectively conveys company message in both written and verbal business development discussions • Continually seeks opportunities to increase customer satisfaction • Approximately 10-20% travel to partners may be required REQUIRED Skills • Undergraduate or masters degree in a biological field (or 2+ years of experience in a position requiring biological knowledge in a pharmaceutical or biotechnology company) and 1+ years of project management experience and: • Outstanding professional written and oral communication skills • Analytical and technical aptitude; ability to grasp a general knowledge of multiple disciplines and technologies • Ability to lead and facilitate multiple activities and resources, motivated and assertive • Good general understanding of business and financial principles • Demonstrated work ethic, integrity, and professional conduct • Strong interpersonal skills • Strong review skills and attention to detail • Proven track record in project management coordinating the efforts of one or more teams • Skilled in the use of Microsoft Project and Microsoft Office (Word, Excel, and PowerPoint) Other Desired Qualifications • Understanding of the pharmaceutical R&D and commercial process and its financial and strategic implications • Experience editing scientific documents • Formal training in Project Management methods and techniques Submission Details • Please email your CV and brief cover letter • Use "Job Code: PM" in the subject line to ensure delivery to the appropriate hiring manager • While we appreciate every applicant's interest, we will only be in contact with the candidates being considered for this position • NO recruiters, please. ]]>

<![CDATA[The Howard Hughes Medical Institute conducts scientific research in leading medical and academic centers throughout the United States. We offer competitive salaries and an excellent, flexible benefits package that includes health, dental and vision insurance, generous personal time off, tuition reimbursement, and employer contributions to a 403(b) retirement program with immediate vesting. We are seeking an organized, detail-oriented, energetic and experienced cell culture/protein biochemistry research technician for an HHMI structural biology laboratory at Harvard Medical School. The primary responsibility will be maintaining and supporting insect cell suspension culture (Hi5 and Sf21/Sf9). Additional duties will include basic molecular cloning, recombinant protein expression in E.coli and insect cells, large-scale protein extraction and column purification, tracking and ordering of lab supplies, and preparation and maintenance of common reagents (e.g. chemicals, competent cells). This position also involves overseeing a Laboratory Aide responsible for washing and sterilizing laboratory glassware. Most laboratory work will be in collaboration with and in support of postdoctoral fellows. The successful candidate will have a bachelor’s or master’s degree and prior, proven experience in cell culture techniques. Requisites also include the ability to multitask while keeping attention to details of scientific experiments and to work independently while effectively operating within a large group. Please send your CV and cover letter to Karen E. Lee, Harvard Medical School, SMB 123, 250 Longwood Avenue, Boston MA 02115. Email: lee@crystal.harvard.edu Fax: 617-432-5600. No phone calls please. Please visit our website to learn more about the lab and its research efforts: <a href="http://crystal.harvard.edu/" rel="nofollow">http://crystal.harvard.edu/</a> <a href="http://www.hhmi.org/" rel="nofollow">http://www.hhmi.org/</a> HHMI is an equal opportunity employer. ]]>

<![CDATA[Seeking a part time employee to manage a songbird breeding facility. Ideally the candidate will be interested in long term employment. Initially, this work will be 10-15hrs a week, on a flexible schedule. (Employee may set their own schedule.) The primary responsibility involves oversight and training of a rotating staff of 3-4 student employees who care for the daily needs of the birds. The students change cages, seed and water, band birds, manage record keeping, and monitor the health status of all birds. The manager will oversee the quality of all of this work, and take initiative to design the best care possible for the birds. The manager must enjoy a detail-oriented work, love taking charge of organization, and be able to inspire good work from student care-takers. Prior experience with animal care, or a general interest in animals is a plus.]]>

<![CDATA[Manage and coordinate data collection and consolidation for the Laboratory of Neuropsychology. Organize and pre-process data and subject lists, perform data entry, identify and fix user errors, manage unstructured data, and write shell scripts and Excel macros to automate tasks and data processing. Perform statistical analysis, including digital signal processing, noise reduction, wave reading, and time series analysis. Integrate data with MATLAB from Filemaker, Excel, text files, and proprietary psychological and physiological software. Acclimate participants to MRI scanner, operate console, give task instructions, and deliver test stimuli using computer. Operate physiological recording equipment and troubleshoot recording and data integrity problems. Assist with and teach research team data management, analysis, and scripting tools. Preferred skills: * Strong Linux and programming skills with MATLAB, shell scripting, database, and Excel VB macros * Experience with database management and consolidation from heterogeneous data sources * Ability to do signal processing, noise reduction, and time series statistical analysis * Knowledge of psychology and neuroscience * Experience with neuroscience, physiological processing, EEG, MEG, EOG, EMG or MRI Please apply to this job via the BU website: <a href="http://www.bu.edu/hr/jobs/open-job-opportunities/" rel="nofollow">http://www.bu.edu/hr/jobs/open-job-opportunities/</a> Refer to tracking code 5142* ]]>

<![CDATA[BioSpace is proud to present the Genetown Career Fair, an opportunity for leading pharmaceutical and biotech companies to meet face-to-face with job seekers. Genetown Career Fair Monday, March 15, 2010 from 11am to 4pm Cambridge Marriott Cambridge, MA Click here for more details and to register! <a href="http://www.biospace.com/jobs/career-fair-detail/?CareerFairId=188" rel="nofollow">http://www.biospace.com/jobs/career-fair-detail/?CareerFairId=188</a> You MUST pre-register online to receive an invitation to attend. Job seekers MUST have a 4-year life science degree and a MINIMUM 2-years of industry experience to attend. If you have a scientific background with industry experience, this is the event for you. Exhibitors are looking for candidates with scientific backgrounds, not business oriented backgrounds. No entry level or internship opportunities available at this event. Do not miss the chance to interview with the biopharmaceutical industry's most prestigious companies! Exhibiting Companies Aerotek Scientific, LLC Alkermes Alnylam Pharmaceuticals, Inc. Broad Institute Cubist Pharmaceuticals, Inc. Decision Resources EMD Serono Genzyme Corporation Integrated Project Management Co., Inc. Ironwood Pharmaceuticals, Inc. (formerly Microbia, Inc.) Lab Pros, Inc. Millennium: The Takeda Oncology Company Millipore Corporation Novartis Institutes for BioMedical Research, Inc. Pfizer Inc. Regeneron Pharmaceuticals, Inc. Tufts Medical Center Vertex All candidates must have at least a four-year college degree and two years of industry related work experience to attend. (Equivalent work experience may be considered in lieu of a four-year college degree.) Qualified candidates will receive their invitations and confirmation numbers via email no later than 72 hours prior to the career fair. Pre-screened and accepted candidates must bring a copy of their invitation with confirmation number to the event. <a href="http://www.biospace.com/jobs/career-fair-detail/?CareerFairId=188" rel="nofollow">http://www.biospace.com/jobs/career-fair-detail/?CareerFairId=188</a> ]]>

<![CDATA[The Research Operations Project Coordinator will provide project development support to the Cardiology Clinical Research and Regulatory Group (CCRRG) in the Department of Cardiology at Children's Hospital Boston. Incumbent makes critical contributions to the development and implementation of key operational systems. Provides development support and critical problem-solving for all projects and work within the CCRRG. Assists Program Manager in the development and implementation of the research operations, quality control processes (including ensuring compliance with Good Clinical Practice), and financial plans. Provides support to key faculty-chaired Research Operations and Projects, including IRB, IND, and IDE applications and renewals, as well as preparations for audits by regulatory agencies such as the FDA. In addition, s/he will assist with academic medical writing activities, including protocols, grants, and manuscripts. A Bachelors degree is required along with at least 5 years of comparable experience. A Masters degree is highly preferred. Experience working with regulatory trials is required. Familiarity with GCP guidelines and FDA regulations on clinical trials would be highly desirable. PLEASE APPLY FORMALLY TO JOB REQUISTION 21000 AT WWW.CHILDRENSHOSPITAL.JOBS.]]>

<![CDATA[EPIDEMIOLOGIST – BEHAVIORAL PSYCHOLOGY RESEARCH & DEVELOPMENT COMPANY Do you want to work with creative, smart, compassionate, innovative people - people with a mission, working together to change health behaviors through technology? If you enjoy being challenged, solving problems and working for the common good, Inflexxion is the place for you. Inflexxion is a respected leader, finding new ways to shape the way people think about health by developing award-winning web-based programs to confront health areas such as pharmaceutical risk management, substance abuse and college health. This is an opportunity to be a part of a company that truly makes a difference in the lives of our consumers. We hire people who work closely with others, are detailed, organized, and understand the project cycle – people who are smart and get things done. We offer competitive salaries and a full range of benefits. We are seeking a Level I Epidemiologist with an interest or background in research on the subject of drug abuse or disease surveillance to join our team on an ongoing, national study to examine prescription drug abuse. The National Addictions Vigilance Intervention and Prevention Program (NAVIPPRO™) is an exciting part of Inflexxion. The Epidemiologist will play an active role in NAVIPPRO’s success through data analysis, report writing and working closely with the team to meet deliverables and deadlines on time and on budget. The ideal candidate should have a master’s degree in epidemiology or public health with demonstrated experience with data management, analysis, interpretation and reporting of public health trends. Responsibilities: • Conduct descriptive epidemiologic analyses of surveillance data regarding substance abuse from both Inflexxion’s proprietary and national data bases. • Monitor and review data from multiple sources with the goal of identifying patterns and trends in prescription drug abuse within defined populations. • Prepare quarterly and annual reports summarizing analyses of surveillance data for pharmaceutical clients. • Write syntax/assist with programming for data analysis for creating client reports. • Assist with management and maintenance of NAVIPPRO databases. • Perform monthly data downloads and quality assurance/quality control checks on data in preparation for analysis. • Assist in survey development and analysis of survey data Qualifications: • MA/MS/MPH, PhD degree in epidemiology or public health or epidemiology and experience conducting public health or social science research. • 2+ years applied epidemiology. • Ability to apply basic epidemiological principles and methods to the analysis of health data, as well as evaluate and interpret epidemiological and statistical data. • Ability to interpret the significance of health and other data obtained from a variety of sources and draw appropriate conclusions. • Experience working with large databases and surveillance data. • Database manipulation skills, with strong attention to detail. • Strong written and verbal communication skills. • Proficient with MS Office Suite applications, including MS Excel and MS Access. • Proficient with SAS and/or SPSS. • Knowledge and experience with ArcGIS and/or SQL is a plus. • Intellectually curious, fast learner, independent worker, detail-oriented. • Work effectively with a multidisciplinary team. To apply, please email your cover letter and resume to: inflexxionjobs@inflexxion.com To learn about other opportunities with Inflexxion, please visit www.inflexxion.com. We look forward to hearing from you. ]]>

<![CDATA[Hepregen Corporation (200 Boston Ave, Suite 1500, Medford, MA 02155, www.hepregen.com) is a venture-backed startup out of the Massachusetts Institute of Technology focused on commercializing a portfolio of liver tissue engineering technologies. Hepregen’s mission is to provide innovative bioengineering solutions to the biotech and pharmaceutical industries in order to improve the success and economics of drug development. Its first product platform (HepatoPaCTM) is a micro-liver platform for advanced toxicity screening and drug discovery. Primary Responsibilities / Reporting Requirements: Implements and runs cell-based assays to characterize and validate liver culture models for screening drug metabolism and toxicity in collaboration with industrial partners. Analyzes data from experiments using statistical software packages. Prepares data summaries for dissemination to the group. Participates in technology development in liver tissue engineering. Exercises judgment within defined procedures to determine appropriate experimental action, and works on problems of moderate scope where analysis of data requires a review of identifiable factors. Works to further refine protocols for cell culture and downstream assays. Reports directly to Director of Research. Degree Requirement / Prior Experience: Bachelors or higher degree in a scientific or engineering discipline with 1-5 years prior experience working in a laboratory, preferably in an industrial setting. Mammalian cell culture experience, especially with primary liver cells (i.e. hepatocytes), is highly desirable. Basic knowledge of cell-based immunoassays (ELISAs, Western blots, colorimetric assays), PCR and aseptic technique using bio-safety cabinets is required. Key Personality Traits: Goal-oriented, highly motivated, strong work ethic, can solve problems with a “hands-on” approach, willing to learn new concepts/ techniques, can communicate research effectively in an interdisciplinary setting, and comfortable working in a start-up environment with an entrepreneurial mindset. Compensation: Hepregen offers competitive pay, a high growth environment, and a benefits package that includes stock options as well as participation in health and dental plans; 401(k) retirement plan; life insurance; and disability coverage. Please send cover-letter and resume to: careers@hepregen.com Hepregen Corporation located at 200 Boston Avenue, Medford MA 02155 is an equal opportunity employer. All candidates must be legally available to work in the United States. ]]>

<![CDATA[Person will be working in a fast paced Clinical Molecular Diagnostics Lab performing a variety of techniques such as: •DNA extraction •DNA Sequencing •Microarray analysis •Troubleshooting and validating assays •Timely delivery of clinical reference lab results to clients, which will include clinicians and collaborative partners •Evaluate test results for completeness, accuracy and quality •Follow and operate in accordance with requirements, policies and procedures Qualifications: •BS degree and 1+ years of molecular biology experience. •Some hands on experience with PCR, DNA extraction, and sequencing is preferred. PLEASE EMAIL RESUMES TO JOBS@ADANTESTAFFING.COM LOCAL CANDIDATES ONLY ALL CANDIDATES MUST BE ELIGIBLE TO WORK IN THE UNITED STATES]]>

<![CDATA[This person will be part of an Analytical Chemistry research team assisting Scientists developing new methods. Qualifications •Candidate will have BS/MS and 1-3 years experience working in an Analytical Chemistry lab. •Some hands on experience working with HPLC. •Awareness of USP dissolution methods •GLP and or GMP experience preferred PLEASE EMAIL RESUMES TO JOBS@ADANTESTAFFING.COM LOCAL CANDIDATES ONLY ALL CANDIDATES MUST BE ELIGIBLE TO WORK IN THE UNITED STATES]]>

<![CDATA[We are seeking a talented, highly motivated team player who will be responsible for producing documents for regulatory submission. Responsibilities for this position: •Produce and/or update Investigator Brochures, clinical protocols, clinical study reports, safety narratives, and correspondence with regulatory agencies in accordance with predefined timelines. •Coordinate production of INDs, BLAs, or NDAs in cooperation with Regulatory Affairs and other team members. Qualifications of the ideal candidate: •B.S., M. S., or Ph. D. in a relevant field. At least 5 years of regulatory medical writing experience and 2 years of pertinent experience in the biopharmaceuticals industry. Experience with producing INDs, BLAs, or NDAs in CTD format is preferred. •Expert working knowledge of ICH E2 and E6 plus CFR 312 and 314. Knowledge of Canadian and/or EU regulatory requirements is preferred. •General knowledge of applied clinical medicine and laboratory interpretation. Experience with large-molecule drug development is preferred. •Advanced knowledge of Microsoft Word, Excel, and PowerPoint. Familiarity with other graphics software is preferred. EMAIL RESUMES TO JOBS@ADANTESTAFFING.COM LOCAL CANDIDATES ONLY ALL CANDIDATES MUST BE ELIGIBLE TO WORK IN THE UNITED STATES]]>

<![CDATA[ AIR Worldwide   <div> </div><div>Would you like to work in a fast-paced , results oriented environment while still maintaining a good work life balance? Work on a wide variety of complex problems that allow for creative and innovative solutions.</div><div> </div>Development and enhancement of natural hazard models (tropical and extratropical cyclones,earthquakes, severe thunderstorm, etc.)<ul><li>Manage the collection and analysis of data; integrate the highest quality data into the modeling process</li><li>Perform validation and verification analysis of implemented model solutions</li></ul>  <ul><li>Ability to gather, understand, and critically analyze data from all relevant sources of natural hazard information</li><li>Solid technical programming skills gained through practical experience (e.g. C, C++, FORTRAN, Python,etc.), FORTRAN experience a big plus</li><li>Familiarity with manipulating large data sets, SQL experience a plus</li><li>Basic knowledge in statistics, familiarity with statistical packages such as R a plus</li><li>Highly motivated and self-directed with demonstrated experience in advancing complex projects</li><li>Excellent verbal communication skills</li><li>Risk modeling experience and/or GIS skills a plus</li></ul>Requirements: <ul><li>2+ years professional experience in a technical environment</li><li>MS degree in Physical Science or Engineering</li></ul> If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=868554-1857-5539" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=868554-1857-5539</a> ]]>

<![CDATA[ Job Title Clinical Laboratory Technologist Department Commercial Laboratory POSITION OBJECTIVE: The Clinical Laboratory Technologist will perform complex molecular-based clinical diagnostic assays and other tasks according to established operational procedures, within our CLIA-certified commercial genotyping laboratory. MAJOR RESPONSIBILITIES AND DUTIES: Purify and analyze DNA samples, using molecular genetics techniques that include PCR. Routinely use liquid handling robotics and analysis equipment to perform genetic assays. Analyze and interpret results which will be used to prepare test reports. Work with Laboratory Manager to review and troubleshoot procedures. Maintain complete documentation for data and results tracking, using our LIMS (Laboratory Information Management System). Adherence to CLIA regulations: equipment maintenance, chemical inventory, sample tracking and SOP review. Other related duties as assigned. SUPERVISION: Reports to Commercial Laboratory Manager. Must be able to work independently with strong attention to detail and results. QUALIFICATIONS: Bachelor’s degree in related scientific area required; 2-4 years of molecular biology experience preferred. Familiarity with concepts, practices, and procedures related to genetic testing and genotyping. Strong attention to detail; precision required. CLIA or GLP laboratory experience preferred. Prior computer experience required. Ability to work well in a team environment required. EOE ]]>

<![CDATA[Provides direct labor for the assembly and dispensing of high quality diagnostic products, and prepares and completes required documentation on manufacturing procedures. Responsible for making operator level decisions regarding the quality of the products manufactured. Qualifications: High school diploma or equivalent required. Must possess and be willing and able to use basic math skills. Should have manual dexterity with attention to detail as well as some mechanical aptitude. Must work well in a group environment. Laboratory working conditions include handling of infectious and non-infectious human plasma, serum and hazardous chemicals. Must be able to lift and carry a maximum up to 40 lbs to per form essential duties of job. Manufacturing experience in a bio-tech company preferred. ]]>

<![CDATA[A research assistant position is available in advanced neuroimaging at the VA Boston Health Care System (VABHCS) in the Jamaica Plain area of Boston. This position is in the new Neuroimaging Research Center at the VA. The candidate will have responsibilities related to patient scanning and data analysis, as well as administrative aspects of the imaging center and ongoing research. The applicant should have some experience in magnetic resonance imaging (MRI) research including some knowledge of one or more common software packages utilized in MRI data analysis (FSL/Freesurfer/SPM), although this is flexible. Some knowledge of Unix/Linux and MATLAB is required. The candidate should be interested in working on studies focused on conditions relevant to the VA mission, including traumatic brain injury (TBI), post traumatic stress disorder (PTSD), cognitive neuroscience of memory, cerebrovascular disease, genetic factors of disease, and age associated decline in cognitive function. The position requires a two-year commitment. The VA is equipped with a 3T Siemens TIM Trio imager and a variety of hardware for stimulus presentation, eye tracking, and physiological monitoring. The VA is an affiliate of Boston University School of Medicine and Harvard Medical School as well as several other academic and health care education institutions and is a site of The National Center for Post Traumatic Stress Disorder (NCPTSD). Interested parties should send a CV and contact information for two references or questions to the Neuroimaging Search Committee at vaimaging at gmail.com. ]]>

<![CDATA[Brigham and Women’s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America’s best hospitals by US News and World Report. GENERAL SUMMARY/ OVERVIEW STATEMENT: Part-time Research Assistant within the Data Coordinating Center for a number of randomized clinical trials. The research assistant will be responsible primarily for data review of all incoming study data in order to determine study randomization eligibility and to report back data inconsistencies to each study site. Additional responsibilities will include maintaining the study randomization databases and the study WWW site, the updating of study protocols and other study resource documents, participation in monthly conference calls with study investigators and staff, and the organization of biannual DSMB meetings. Other responsibilities will include assisting of the Data Manager on a number of tasks: training and supervising of additional staff on data entry procedures, generation of trial monitoring reports for study investigators, periodic cleaning and data audits of all study data, and creating data archives and data codebooks. Excellent organization skills and attention to detail are required. PRINCIPAL DUTIES AND RESPONSIBILITIES: 1. Will maintain the study protocols and related documents, and data collection forms. 2. Review all completed study collection forms for quality control issues (checking for completeness, accuracy and any data inconsistencies). Communicate data discrepancies to study staff in a timely manner. 3. Record and communicate assignment of diet randomizations for eligible participants. Maintain randomization and data tracking databases. Create spreadsheets of follow-up appointments for enrolled study participants for dissemination to study staff and for incorporation into study datasets. 4. Upload documents and create updated html images of the study¿s public and private WWW sites. 5. Under the direction of the Data Manager, the Research Assistant will: a) Help produce monthly and quarterly trial monitoring reports for study investigators, the study¿s Data Safety Monitoring Board, and for the NHLBI Project Officer. b) Maintain study databases by performing periodic downloads of data and concatenation of data files. c) Create study data archives (SAS), perform periodic data audits, and distribute study data documentation through study codebooks. d) Train and supervise work study staff as needed on the use of the data entry system (MS Infopath) and the study databases (MS Access, MS Excel, and MySql). 6. Participate in periodic conference calls with study investigators and other staff. Record the minutes of these calls for dissemination. Maintain conference call calendars and schedules. 7. Organize biannual DSMB meetings. Contact DSMB members to schedule in-person meetings and conference calls. Disseminate meeting materials prior to the event, and record meeting minutes at the events. QUALIFICATIONS: Bachelor of Arts/Science degree. Minimum of 1 year experience in a related field. Three years of experience in a related field preferred. SKILLS/ ABILITIES/ COMPETENCIES REQUIRED: Experience with word processing and data management (MS Access and Excel). 1. Experience with SAS statistical software preferred. 2. Experience with MS Infopath , XMLSpy, and MySql software helpful 3. Strong organizational skills to do multiple tasks. Must be detail oriented. 4. Excellent interpersonal skills necessary in order to communicate effectively with study DSMB members, investigators and other staff. 5. Supervisory skills preferred. Shift Day Shift To apply online, please submit your resume here: <a href="https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2198632" rel="nofollow">https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2198632</a> Brigham and Women’s Hospital is an EEO, AA and VEVRAA employer. <a href="http://www.brighamandwomens.org/careers" rel="nofollow">http://www.brighamandwomens.org/careers</a> ]]>

<![CDATA[Brigham and Women’s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America’s best hospitals by US News and World Report. GENERAL SUMMARY/ OVERVIEW STATEMENT: Works under the very general direction of the Principal Investigator and Division Administrator, performs full scope of management responsibilities in a research laboratory, including inventory management, purchasing of supplies and equipment, research animal issues, budget preparation, compliance with regulatory agencies/bodies, safety activities, and overseeing the day to day staff activities, including orientation and training to lab protocols, techniques, etc. Under the direction of the PI, independently performs sophisticated experiments and participates with the principal investigator in the design of experimental protocols. Interprets experimental results in conference with other researchers. PRINCIPAL DUTIES AND RESPONSIBILITIES: 1. Lab Management Responsibilities: a. Responsible for financial management of laboratory supplies. Develops supply budgets, analysis trends, and produces reports. Oversees use of laboratory funds and supply usage. b. Responsible for coordination of all regulatory and compliance activities for the laboratory, including all safety, infection control, animal facility access and use, etc. c. Oversees staff activities. Coordinates general lab duties between self and technical research assistants. Assists in training, orienting, and advising of other research staff on availability and location of general lab supplies, lab procedures and technical protocols as necessary. d. Oversees general lab operations and maintenance: equipment upkeep, ordering supplies, animal purchase and maintenance. Assists in planning and development of long-term lab equipment and other needs. e. Assists division administrator in grant budget management. f. Assists in development and maintenance of laboratory policies and procedures. 2. Research Technician Responsibilities: a. Carries out independent research projects. Designs research protocols along with research associates. Collects data through use of laboratory techniques. Maintains complete and accurate record of experimentation, including careful documentation of all work and procedures. b. Researches new experimental techniques and technologies and improves upon existing protocols. c. Participates in all aspects of grant writing and proposals. d. Organizes, calculates and interprets data using general statistical tools and basic bioinformatics tools. Prepares handouts, figures, tables, and slides for lectures. Prepares and organizes data method and results for laboratory presentation. Reports on work in progress at lab meetings and conferences, and interprets experimental results in collaboration with other researchers. e. Independently/In collaboration with research associates writes scientific research manuscripts/publications/articles. SUPERVISORY RESPONSIBILITY: 1. Supervises combination of 2-6 doctoral students, post-doctoral fellows and junior technicians in the use of specialized laboratory equipment and techniques. 2. Supervises day to day staff activities. 3. Assists in the training and orientation of laboratory employees. FISCAL RESPONSIBILITY: 1. Keeps an account of laboratory supply purchases on related funded grants. 2. Assists in grant fund management. 3. Maximizes economical expenditure of research grants on capital equipment, laboratory supplies, and consumables. QUALIFICATIONS: 1. BS or equivalent degree, or significant directly related work experience required. 2. Minimum of 5 years of progressively more responsible research work experience. SKILLS/ ABILITIES/ COMPETENCIES REQUIRED: 1. Must be able to make independent, effective decisions in appropriate situations. 2. Must possess a scientific imagination commensurate with the independent execution of research projects. 3. Must have aptitude for technical problem solving. 4. Ability to effectively supervise others. 5. Excellent organizational skills to ensure smooth functioning of lab. 6. Demonstrated analytical skills and ability to logically sequence experiments to maximize research. 7. Must possess aptitude for budget management. 8. High level of computer literacy. 9. should have experience in performing following methods: isolation of immune cells from spleen, blood, kidney, and heart, flow cytometry, mixed lymphocyte culture, ELISA, ELISPOT, immunohistochemistry on paraffin and frozen sections, real time RT-PCR, Luminex, WORKING CONDITIONS: 1. Normal laboratory environment. 2. May work with and/or be exposed to radioactive and other hazardous materials, under controlled conditions. Shift Day Shift To apply online, please submit your resume here: <a href="https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2198749" rel="nofollow">https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2198749</a> Brigham and Women’s Hospital is an EEO, AA and VEVRAA employer. <a href="http://www.brighamandwomens.org/careers" rel="nofollow">http://www.brighamandwomens.org/careers</a> ]]>

<![CDATA[Brigham and Women’s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America’s best hospitals by US News and World Report. PRINCIPAL DUTIES AND RESPONSIBILITIES: 1. Implementation of Projects ¿ Direct and Oversees the daily operations of all research activities. ¿ Represents the project(s) to NIH, contractors, subcontractors, sponsoring agencies, and other entities ¿ Develops and maintains a Quality Assurance Program to track progress in all areas and ensures proper implementation at all sites ¿ Troubleshoots research and administrative issues and problems raised by sponsors, funding agencies, collaborators, and staff ¿ Remains knowledgeable about changing federal research guidelines to insure full compliance ¿ Manages research assistants, clerical staff, and recruitment personnel. Responsibilities may include, , recommend hire/fire, disciplinary action, performance evaluation, etc. ¿ Supervises community education efforts, new subject recruitment ¿ Orients and trains new staff in clinical research procedures. ¿ Prepare NIH submission material for annual renewals of acting grants as well as submission of new grants working with the Director. ¿ As part of the leadership team, participates in and coordinates the planning, development, and implementation of research protocols in accordance with research parameters set out by the principal investigator. ¿ Conducts the scheduling and implementation of day-to-day clinical activities and procedures, ensuring efficient workflow and adequate care and treatment of research subjects. ¿ Plans and carries out programs for the recruitment, screening, enrollment, and retention of research subjects and/or volunteers; instructs subjects on treatment methods and protocol. ¿ Establishes appropriate data collection systems and procedures, according to research protocol; completes and monitors the collection, processing, and recording of clinical data and/or specimen samples, as required by established protocol. ¿ Ensures that all clinical activities are carried out in accordance with established research protocol and within acceptable clinical procedure and safety standards. 2. Network Communication ¿ Works with research collaborators to implement and operationalize studies conducted within the Harvard HIV Vaccine Trials Unit (HVTN), overseeing activities at Fenway Community Health Center (FCN), and BIDMC ¿ Review project-specific systems to enhance project efficiency ¿ Attends all regularly scheduled research meetings, trainings, forums, HVTN meetings, and FCH staff meetings ¿ Promotes and facilitates communication and discussion among staff regarding changes in protocol procedure and other pertinent information ¿ Responsible for ensuring on-going IRB approval for grants and studies. 3. Writing ¿ Assists in developing procedures and updating as needed ¿ Assist in the drafting of informed consents and other documents ¿ Assists in the review and submission of research proposals ¿ Assist in the development of materials to support recruitment activities ¿ Prepares project reports Will manage / supervise approximately 10 research staff. Performs all other duties/responsibilities as needed. QUALIFICATIONS: BS required; Masters Degree preferred 7-10 years of clinical research experience required. Infectious Diseases and/or oncology experience preferred. Prior management experience preferred SKILLS/ ABILITIES/ COMPETENCIES REQUIRED ¿ Minimum 7 years directly related experience ¿ Must have good interpersonal skills and the ability to supervise others ¿ Must possess excellent organizational skills ¿ Must possess excellent written and oral communication skills ¿ Must have basic knowledge of accounting and financial management procedures ¿ Basic knowledge of the translational research process, specifically Phase I, II, and III clinical trials preferred ¿ Flexibility in a fast-paced environment ¿ Ability to identify potential problems and develop solutions to problems ¿ Knowledge of the principles and procedures of clinical research. ¿ Organization and coordination skills. ¿ Ability to design and implement systems necessary to collect, maintain, and analyze data. ¿ Knowledge of FDA regulations and guidance¿s. ¿ Strong interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in a diverse community. WORKING CONDITIONS: The Senior Project Manager will supervise the conduct research protocols under the HVTN and Infectious Disease Oncology Programs and in the outpatient/inpatient setting of the Division of Infectious Disease, BWH/DFCI. New hires to the Division of Infectious Disease will share office space typical for a hospital/clinic environment. Shift Day Shift To apply online, please submit your resume here: <a href="https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2198954" rel="nofollow">https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2198954</a> Brigham and Women’s Hospital is an EEO, AA and VEVRAA employer. <a href="http://www.brighamandwomens.org/careers" rel="nofollow">http://www.brighamandwomens.org/careers</a> ]]>

<![CDATA[Brigham and Women’s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America’s best hospitals by US News and World Report. The Surgical ICU Translational Research (STAR) Program at Brigham and Women's Hospital is a collaborative research center focusing on clinical and outcomes research topics in Critical Care Medicine. Modeled after the multidisciplinary approach to Critical Care Medicine, our clinical research activities focus on topics in surgical, anesthesia, emergency medicine, infectious diseases, renal and pulmonary medicine. Our mission is to develop innovative preventative and treatment strategies for critical care by developing and managing high quality investigator initiated and industry sponsored clinical trials. We are currently looking for a clinical research assistant to identify, recruit and conducting interviews with elderly patients for a large multi-project, multi-site study The role will also involve collecting, documenting, and organize participant data. PRINCIPAL DUTIES AND RESPONSIBILITIES: 1. May coordinate all or portions of research study activities. Functions as a resource for study issues for research staff, fellows, and MDs. Identifies & consents patients, collects and processes samples, and collects and maintains data integrity for the studies. 2. Provides support and assistance to other research assistants. May provide training and guidance to volunteers, sponsored staff. 3. Designs, implements and evaluate recruitment strategies for study participants. 4. Interacts with patients / subjects with regard to clinical research studies. This includes interacting with patients and families, screening patients, ensuring they meet appropriate criteria, and making judgments both independent and in collaboration with MDs as to the suitability of specific patients. May serve as a liaison with patients and physicians. 5. Collections and organizes participant data by interview, patient assessment and medical record review. 6. Will receive training in interviewing techniques, neuropsychological assessments and phlebotomy if required 7. Some travel to patient homes for interviews and assessments may be required. 8. Responsible for maintenance, and updates of clinical research databases. Responsible for data validation and quality control, data entry into CRFs, if applicable. May be required to input data. 9. In conjunction with Research Manager/Principal Investigator, develops and implements new research protocols including design, data collection systems and institutional review board approval. 10. Implements and maintains quality assurance procedures and systems 11. Communicates regularly with the Research Manager and PI(s) about all aspects of the research trial. 12. Ensure that knowledge about regulatory requirements are current by reading and attending local seminars related to policy and regulatory issues (FDA, NIH, IRB, etc.) 13. In collaboration with Research Manager and PI, prepares and may present certain portions of presentations. This may include preparation of articles for publication. 14. All other duties, as assigned. QUALIFICATIONS: BS OR BA Previous work or volunteer experience in clinical research or in a clinical care setting. Preferably experience in actively coordinating research trials with an elderly population. Sound independent judgment and competence in research methodologies. SKILLS/ABILITIES/COMPETENCIES REQUIRED: ¿ Ability to work independently. ¿ Excellent interpersonal skills are required for working with the study participants. ¿ Good oral and written communication skills. ¿ Analytical skills and the ability to resolve technical or research problems and issues and to interpret the acceptability of data results. ¿ Knowledge of clinical research protocols. ¿ High degree of computer literacy. ¿ Excellent organizational skills and ability to prioritize a variety of tasks. ¿ Careful attention to detail. ¿ Ability to demonstrate professionalism and respect for subjects rights and individual needs. ¿ Knowledge of data management programs. ¿ Coordinator certification preferred Shift Day Shift To apply online, please submit your resume here: <a href="https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2198997" rel="nofollow">https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2198997</a> Brigham and Women’s Hospital is an EEO, AA and VEVRAA employer. <a href="http://www.brighamandwomens.org/careers" rel="nofollow">http://www.brighamandwomens.org/careers</a> ]]>

<![CDATA[JOB SUMMARY: The QC SR Chemist is responsible for performing routine and non-routine cGMP analytical chemistry assays of raw materials, in-process samples, finished formulations, stability testing and method qualification. JOB RESPONSIBILITIES: 1. Performance of analytical testing for incoming, inprocess and final products, and stability samples. 2. Performance of raw material monograph testing. 3. Performance of QC analytical chemistry assays, HPLC, GC, IR. 4. Performance of wet chemistry assays. 5. Performance of QC analytical instrument maintenance, calibration, and validation. 6. Performance of QC general laboratory equipment maintenance. 7.P erformance of QC method qualifications and validations. 8. Performance of cleaning validation studies. 9. cGMP data documentation, reporting and review. 10. Involved in OOS and departure investigations. MINIMUM REQUIREMENTS FOR EDUCATION, TRAINING AND EXPERIENCE: 1. Must be skilled in the use of computers and proficient is the use of word processors, and spreadsheets. 2. Must have strong organizational skills and ability to prioritize and multi-task. 3. Bachelor's degree in a scientific discipline. 4. Minimum of 3 years industry experience in a GMP or GLP environment. 5. Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus. MANAGERIAL & SUPERVISORY RESPONSIBILITIES: Not Applicable The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. ]]>

<![CDATA[The person in this position will be responsible for the design, development and implementation of bioanalytical assays (PK, immunogenicity, biomarker, activity assays) in support of the Hemophilia Development Programs. Responsibilities will include assay development and qualification/validation of appropriate assays to detect protein therapeutics and immune responses in support of preclinical and clinical studies in accordance with current industry guidelines and standards. The successful candidate will have demonstrated experience in the bioanalytical area, have an interest and aptitude to learning new technologies, pay attention to details, and have a strong work ethic to meet demanding time lines. In addition, the candidate needs to possess excellent written and verbal communication skills. Qualifications: 3+ years of industry experience in a related field. Experience in immunoassay development, and immunogenicity assays using techniques such as ELISA, MSD, PCR, and statistical analysis of the data are required. Familiarity supporting preclinical and clinical studies and with PK/immunogenicity/PD concepts is desirable, as well as with GLP compliance. About Biogen Idec: Transforming Discovery into Care With operations across the Americas, Europe, and Asia, Biogen Idec (NASDAQ:BIIB) is one of the world's leading biotechnology companies, creating new standards of care in oncology, neurology, and immunology. Every day, employees of Biogen Idec make a difference in people's lives, through pioneering research and development, manufacturing, and our worldwide commercial capabilities. Learn more at www.biogenidec.com/careers. Biogen Idec is proud to be an equal opportunity employer. To apply for this position, please <a href="http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R9621275608147" rel="nofollow">CLICK HERE</a> ARBBIO054-736506]]>

<![CDATA[Thoughtful Science. Tailored Solutions. NERI is a full-service Contract Research Organization that provides customized, global clinical trial solutions and registry services to pharmaceutical, biotechnology, biomaterial, and medical device companies. NERI also has notable experience collaborating on federally-funded research with organizations like the National Institutes of Health. Since its founding in 1986, NERI has earned widespread recognition for its scientific credibility, efficiency, and expertise in the successful conduct of clinical trials. We are currently looking for a Clinical Research Associate. In that position, the Clinical Research Associate will: <li> Function as the primary contact for site coordinators, clinicians and interviewer in regards to protocol, contracts and payments; <li> Requests, updates and maintains regulatory files for each clinical site; <li> Performs all aspects of remote monitoring of clinical sites; <li> Actively participate in training sessions, meetings and conference calls. Trains clinical sites on registry protocol via webinar; <li> Develop and update training and procedure manuals as needed. Qualifications: <li> M.S. degree in a related field plus one year of research experience; or a B.S. degree in a related field (or RN) and three years of clinical experience of which one year is in research; or Bachelor’s degree in a clinical discipline plus a MPH. <li> Ability to work independently, initiate and implement appropriate quality control procedures and monitor and coordinate multi-site research trials; <li> Excellent oral and written communication skills. Foreign language skills in Spanish, Italian, German, Swedish or Dutch would be helpful; <li> Demonstrated ability to work independently. If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com <hr> NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V ]]>

<![CDATA[<big><center>At EMD Serono, Inc. our strength is our people!</big></center>About the CompanyEMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.Description<ul><li>Manage the Environmental Health and Safety Department of EMD Serono including the EHS Crisis management program at our Billerica campus.<li>Identify and reduce EMD Serono's business risk, including protecting all employees, contractors, visitors and guests and our assets.<li>Deliver new industry recognized EHS policies, procedures ,and programs including compliance measures in conjunction with the EHS Director and Merck KGaA, Darmstadt, EHS department.<li>Raise the profile of the EMD Serono EHS safety culture and drive its EHS reputation internally and externally.<li>Establish EHS KPIs that can effectively measure the effectiveness of EHS activities.</ul>Key Tasks & ResponsibilitiesManagementDevelop and Drive all Environmental Health and Safety ( EHS) and Crisis management policies, procedures, programs and activities including R&D Lab Support activities at our Billerica site:<ul><li>Deliver in collaboration with the EHS Director a new EHS Strategy and Business model to increase our Safety profile while protecting the business and increase compliance.<li>Manage the EHS team and the laboratory support staff, to ensure all operations are consistently carried out within agreed EHS policies and procedures.<li>Responsible for all EHS activities for our Billerica site.<li>Ensure compliance with regulatory, federal and state laws and advise on legislation and prepare and implement policies and procedures to support requirements.<li>Lead internal and external corporate EHS audits and coordinate site visits.<li>Drive the local EHS Crisis Management planning and coordinate activities with the crisis manger and the Senior Leadership Team.<li>Implement and drive compliance by standard operating procedures by develop "best in class" practices.<li>Introduce KPIs to measure the success of EHS from the customer and employee base.<li>Drive new industry leading key EHS safety programs to support our construction management partner on our major construction project at the Billerica site including a new R&D centre of excellence and a validated process building conversion.<li>Responsible for monitoring and implementing best practices consistent with Federal, State and local laws. Ensure overall compliance and commitment to environmental practices and deploy effective policies and procedures.<li>Implement policies and procedures to ensure that practices are in compliance with the appropriate statutes and regulations, and that regulatory reporting requirements are met.<li>Ensure that inspections are conducted, corrective actions are completed on time, and all findings are documented correctly within specified timelines.<li>Investigate and resolve environmental concerns, or complaints received from within the organization, government regulatory agencies, etc.<li>Develop and implement programs designed to increase employee awareness and knowledge of safety, compliance policies, and corporate procedures.<li>Review current policies, procedures, and documentation for compliance with government laws and regulations and make necessary changes accordingly.</ul>ISO 14001 Program<ul><li>Maintain and develop effectiveness of the Environmental Management Systems (EMS), policies and procedures.<li>Manage EHS sustainability programs and improve the company's envoi mental performance by effective measurements.<li>Introduce intuitive laboratory and environmental policies and procedures to reduce risk and protect company operations, assets and personnel.<li>Manage the health and safety and laboratory support staff to ensure R&D efficiency.<li>Lead and coordinate company responses with federal, state and local environmental inquiries.<li>Coordinate and drive solutions with environmental regulatory agencies to minimize impact and compliance.<li>Manage the Facility Environmental Safety and Health program to ensure safe workplace conditions.<li>Recognize, evaluate and control environmental factors or stresses arising in or from the workplace or facility that may cause sickness, impaired health or well being, or significant discomfort and inefficiency among employees.<li>Coordinate monitoring of all workplace environments throughout all EMD Serono facilities.<li>Develop and deploy EHS auditing programs within the company, complete written reports and findings and recommend improvements to the Director of EHS and Facilities.<li>Support the FM Operations Manager on risk assessments and audits.<li>Proactively identify hazards in the workplace conditions and take preliminary action to correct and communicate areas of improvement.<li>Protect employees by monitoring, revising work procedures, training, and requiring use of protective clothing and personal protective equipment.<li>Deploy effective and measurable EHS crisis management programs ,deliver a clear EHS communication plan.<li>Take effective steps to ensure that workplace conditions comply with applicable federal and state occupational safety and health standards.<li>Participate in Occupational Safety and Health Administration (OSHA) inspections and in any procedures that may follow a work related incident.<li>Investigate, prepare, and forward as required reports on injuries and compliance issues to management.<li>Drive employee health and safety orientation and training programs.<li>Deliver solutions to support continuous improvements in all areas under this role.</ul>Manage the team to control use of radioactive materials, protect and support the heavy chemistry and vivarium R&D operations, irradiators and X-Ray Crystalography operations by driving "best in class procedures" to protect against related hazards.<ul><li>Maintain policies and procedures to comply with state mandated record checks, and associated management of source use.<li>Develop policies and procedures for inspection standards, decontamination procedures, emergency procedures and waste handling.<li>Implement control protocols to limit personnel radiation exposures, environmental releases, and surface-type contaminants.<li>Compliance with federal, state, local, and industry radiation protection regulations and ensure that radiation levels are in compliance with permissible standards and in keeping with ALARA (as low as reasonably attainable) philosophies.<li>Develop and train "best in class" training programs for radiation training and monitoring programs.<li>Implement a training program to ensure a coordinated approach to regular training compliance is maintained.</ul>Accountability<ul><li>Engineering/Facilities/EHS Departments.<li>Research and Development operations.<li>All company locations in the U.S. (including field safety).</ul>Functional Knowledge<ul><li>Proven Leadership and industry track record to drive Environmental Health and Safety programs including Crisis management planning, ergonomics, chemicals, biologics, radiation, hazardous waste, environmental practices, policies, laws, codes and emergency responses.</ul>Business Expertise<ul><li>Proven track record and industry expertise of BioPharma EHS field.<li>Solid understanding of business practices and needs as related to both laboratories and office space.<li>Environmental Health and Safety to best in class practices.<li>Construction safety practices and management.<li>OSHA certifications.</ul>Leadership<ul><li>Manage direct reports supporting Research & Development, and all safety related business functions.<li>Ability to guide, consult and influence others regarding all matters of employee health & safety.<li>Excellent communication skills and presentation skills are key to this role.</ul>QualificationsEducation<ul><li>MBA or Master's Degree in the field of EHS laboratory and business operations.</ul>Professional Skills, Qualifications & Experience<ul><li>Minimum of 10-15 years experience in EHS BioPharma organizations.<li>Proven EHS management role.<li>Proven knowledge of OSHA standards, and Federal, State and local environmental laws, codes, programs, practices and policies.<li>Thorough understanding of Research Operations and GMP.</ul>Competencies<ul><li>Excellent organizational, communication, interpersonal and relationship building skills.<li>Strong problem analysis and solving skills.<li>Travel required, including visits to US Corporate Headquarters in Rockland MA and other facilities and occasional visits to Merck KGaA, Darmstadt, Germany.</ul>Click the link below and open the door to the future by submitting your resume today!<li><a href="https://merckgroup.taleo.net/careersection/2/jobdetail.ftl?lang=en&job=1000325" rel="nofollow">EMD Serono 1000325</a></li></ul></div><div> </div></div> Awards & RecognitionJune 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work! May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries! October 2008, EMD Serono Named as a Top Employer by Science Magazine!</big><ul><li><a href="http://www.emdserono.com/en/who_we_are/awards_and_recognition/awards_and_recognition.html" rel="nofollow">more</a></li></ul><div></div><a href="http://www.emdserono.com/en/who_we_are/awards_and_recognition/awards_and_recognition.html/%E2%80%9D%3Emore%3C/a%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv%20class=" rel="nofollow"> </a> ]]>

<![CDATA[Premier Research is a leading global solutions-driven CRO committed to therapeutic focus and operational expertise to deliver clinical trial services of the highest quality for biopharmaceutical and medical device companies. POSITION SUMMARY: PDM is the single point of contact in GCDS for the CPM. PDM is accountable for all data management activities. Assists in the development and implementation of new standards. Ensures data management project plan details are consistent with program level plans and milestones. Mitigates/arbitrates technical and process issues between outsourced partners. Ensures that the data management plan and cleaning strategy are consistent across the program. Serves as point of contact for internal and external audits. Ensures data flow across the program is within projected timelines. Ensures consistency in review and quality of safety data across the program. Reviews data quality audit outputs to identify trends across the program to ensure quality data. Reviews metrics and monitor performance against targets. Apply lessons learned to continuous improvement of data management practices within a program. PRIMARY JOB FUNCTIONS: •Focuses on quality of deliverables as well as the oversight of the DM activities at the program level (and protocol level where necessary) •Ongoing review of those items included in the Oversight plan •Support and guidance to LDM through ongoing activities •UIMS requests at early design stage (prior to LDM assigned) •Issues escalation from LDM (such as the team members not providing input in set timeline eg CRF review/comments) •Works directly with the CPM to ensure they have the support needed in their day to day interactions with the FSP for DM activities •Ensures the CPM is getting feedback from the LDM •Ensures the team is getting their outputs (clinical review listings etc) on a regular basis •Acts as the Single POC for all GCDS services at the Program level •Acts as the face of GCDS for their program or TA •Ensures consistency and quality of the data management activities across the TA/ program •Reviews use of TA standards across a program to ensure consistency •Trains and follows sponsor’s Standard Operating Procedures as applicable EDUCATION/SKILL/EXPERIENCE REQUIREMENTS: •Bachelor’s or equivalent degree preferred •Must have a minimum of 5 years of data management experience •Prior project management experience preferred •Experience working on multiple projects simultaneously •Experience with Oracle Clinical preferred For Immediate Consideration contact Kaitlin O'Mara at kaitlin.omara@premier-research.com or 617-237-1139 ]]>

<![CDATA[A Research Assistant (Technician) position is available in a laboratory at Brandeis University to study neuronal development and function. Job responsibilities include: - maintaining the lab strain collection - general lab maintenance including ordering supplies - performing an independent or supervised research project Qualifications: A Bachelor’s degree in Biology or related sciences and some prior lab experience in molecular biology or genetics is required. A minimum of a two-year commitment is required. Start date is preferably around June 1, 2010. How To Apply: Submit cover letter and resume as a single document at <a href="http://www.brandeis.edu/humanresources/jobs/external.html" rel="nofollow">http://www.brandeis.edu/humanresources/jobs/external.html</a>. Elect option for "External Applicant". Sort the job listing by clicking the Job ID column heading. Locate the desired job listing. Click the job title and then Apply Now. Closing Statement: Brandeis University operates under an affirmative action plan and encourages minorities, women, disabled individuals, and eligible veterans to apply. It is the policy of the University not to discriminate against any applicant or employee on the basis of race, ancestry, color, religion, sex, sexual orientation, age, genetic information, national origin, disability, veteran status, or on the basis of any other legally protected category. ]]>

<![CDATA[ngstrom Advanced has a paid internship position available as a Technical Support Staff. This job description will consist of learning and assessing the issues with instruments if and when they occur. We are looking for someone who is a quick learner, and also isn’t afraid to step and take initiative. This position will eventually lead to the Sales of the instruments as well, so we are looking for someone who can communicate and close sales as well as being a technical support agent. Angstrom Advanced is a small company therefore we are looking for someone who is motivated and understands that their work directly influences the success of the business, therefore we understand the importance of someone who will assist and be a good addition to the team. Angstrom Advanced Inc. is a High Tech company that specializes in the Sales and Support of Scientific Analytical Instrumentation. Our product list consists of measuring devises mainly utilized in the nano-technology sector of the industry. We are looking for an individual who is: • Must Have a Major in engineering fields • Hard Working – Not afraid to think outside of the box • Strong capabilities in speaking with potential customers and closing deals • Technical – Fast learner and has experience in dealing with various products • Honest • Intuitive We do not take phone calls for this Job Offer. Please send all resumes and questions to Sales@angstrom-advanced.com ]]>

<![CDATA[Technical Assistant I - Reddien Lab The Whitehead Institute for Biomedical Research is a leading, nonprofit research and educational institution that has defined the cutting edge of biomedical science, creating a legacy of research excellence and academic eminence since 1982. Wholly independent in its governance, finances and research programs, Whitehead shares a teaching affiliation with Massachusetts Institute of Technology (MIT), offering the intellectual, collegial and scientific benefits of a leading research university. Whitehead’s Faculty Members and Fellows run pioneering programs in cancer research, immunology, developmental biology, stem cell research, regenerative medicine, genetics and genomics—programs with a record of success. Director David C. Page likens the Institute to an artists’ colony. “What we do here at Whitehead is attract the best possible intellectual capital and empower maximally creative—really wildly creative—individuals to realize their dreams within these walls”. Whitehead offers a generous comprehensive benefits package which includes health and dental plans, retirement program, paid time off, reimbursement accounts (FSAs), short and long term disability and much more. OVERALL RESPONSIBILITY Performs bench level experiments and small independent research projects to support scientific research objectives of the Reddien lab. The Reddien Lab works on the regenerative biology of planarians and uses methodologies sucha s RNAi, in situ hybridizations, microarrays and antibody labeling to study the stem cells of planarians. Analyzes experimental data, addresses methodological problems in experimental protocols and results, and reports data to supervisor. CHARACTERISTIC DUTIES * In consultation with the Principal Investigator or other project manager, conducts bench level experiments and small independent research projects. * Operates lab equipment and prepares and orders necessary supply stocks. May work with vendors to address equipment, reagent, or supply issues. * Documents, compiles, and assists in interpreting experimental data. Reports data to supervisor in oral and written reports. * Operates and maintains laboratory equipment to complete investigations. * Prepares, orders, and maintains stocks of necessary reagents, solutions and supplies. * May consult scientific literature as needed. * Other tasks as required or assigned. QUALIFICATIONS * Bachelor’s degree in biology or a field directly related to the work. * Proficiency in basic lab techniques and principles of molecular biology required. * Knowledge of various scientific databases and publications preferred. * Excellent written and oral communication skills, strong organizational skills required. Interested candidates should send resume to: resumes@wi.mit.edu 9 Cambridge Center Cambridge, MA 02142 ]]>

<![CDATA[JOB TITLE: Anatomy Lab / BioSkills Technician STATUS: Full-Time JOB DESCRIPTION: The Anatomy Lab / Bioskills Technician’s primary responsibility is to ensure customers’ labs run as smoothly and efficiently as possible. The Anatomy Lab / Bioskills Technician works closely with physicians and researchers during labs, receiving & preparing specimens, setting up the lab including proper positioning & draping of the anatomical specimens, assisting during the course, proper repackaging and shipping of specimens and cleaning of lab and instruments. Positive, can do attitude, outstanding problem solving skills, attention to detail, strong communication skills, full time travel and knowledge of anatomy are a must. Previous anatomical specimen lab or “wet lab” experience a plus. SPECIFICATIONS: • Be accountable for OSHA compliance o Ensure proper disposal of biohazard materials • Maintain adequate surgical and lab supplies for your personal bin. • Must be extremely flexible team player, adaptable to constant change. • Excellent customer service abilities. Anatomy Lab / BioSkills Technician must be able to: • Stand for extended periods of time. • Lift up to 70lbs. • Speak English clearly and fluently • Complete tasks using computer software at an average skill level • Provide excellent customer service via all instruments of communication • Comfortably interact with researchers and physicians. REQUIREMENTS Education Bachelors Degree with emphasis on Anatomy/Physiology or verifiable work experience in related field. Experience Clinical / Anatomy BioSkills Lab experience preferred. Please send Cover Letter, Salary History, and Resume for consideration. ]]>

<![CDATA[<center>At EMD Serono, Inc. our strength is our people!</center>About the Company EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts. DescriptionEMD Serono is seeking to appoint a motivated and well qualified scientist for the Protein Engineering and Monoclonal Antibody Technologies (PEAT) group within New Biological Entities (NBE) Technologies. He/she will be responsible for the Monoclonal Antibody Engineering needs of the group and head up a laboratory staff of three with a potential to grow.This individual will report to the Head of PEAT at their facility in suburban Boston and will be part of an energetic team in a key strategic area of the Discovery organization within EMD Serono. In this regard, he/she will play an important role in the overall responsibility of NBE Technologies for the discovery, optimization and progression of the Company's biotherapeutics discovery pipeline.As Scientist - Antibody Engineering the incumbent will have responsibilities including, but not limited to, the following:<ul><li>Leading a group of scientist and technicians in the Monoclonal Antibody Engineering laboratory</li><li>Assuming responsibility for the humanization and optimization of antibody candidates generated by hybridoma- or phage display-technology.</li><li>Managing the group and taking responsibility for its projects by driving and coordinating his/her direct reports in achieving the specific objectives of the respective research projects.</li><li>Advancing antibody technologies within his/her own group as well as influencing the strategies on current and future technologies.</li><li>Representing the monoclonal antibody department in specific antibody project teams.</li><li>Taking responsibility for defining requirements for research projects and identifying potential constraints and risks.</li><li>Use of problem solving skills in evaluating issues, and monitoring and initiating corrective actions where necessary.</li><li>Taking responsibility for proposing new projects or amendments to existing projects to the Head of PEAT in the US.</li></ul> Qualifications<ul><li>The ideal candidate will have a Ph.D. in molecular biology, biochemistry, biotechnology or biological sciences.</li><li>This individual will be a highly motivated scientist with a proven track record in antibody engineering and must have several years of post-doctoral experience in an academic or industry setting.</li><li>A strong background in molecular biology, with extensive experience in antibody engineering, antibody expression and purification, and biochemical and biophysical methods for the analysis of antibodies is required. An interest to work part-time at the laboratory bench is desirable.</li><li>Familiarity with antibody phage display technology and affinity maturation, and interpretation of computational modelling of antibody-antigen interactions would be useful. Further, experience in preclinical development of therapeutic antibodies is desirable.</li><li>It is desired that the candidate demonstrate an aptitude to interact constructively with others across multiple cultural backgrounds in a dynamic matrix structure. He/she must have the ability to collaborate with colleagues throughout the organization in research functions i.e., bio-informatics, protein and cell sciences and structural biology and in corporate functions i.e., business development, intellectual property.</li><li>Further to this the candidate will possess strong communication skills, both oral and written. He/she should be confident in presentation with parties both small and large.</li><li>As leader of a group, the candidate must be committed to its members and foster a teamwork approach. This will partially be accomplished through the facilitation of a positive work environment. He/she should be skilled in motivating and coaching others as well as interacting well in a team.</li><li>The candidate will be, above all, a proactive self-starter with a positive "can do" attitude. He/she will have demonstrated success in achieving goals, be strongly results oriented and have the ability to drive tasks through to completion.</li><li>The incumbent will be required to focus on multiple issues at one time, and must have the ability to organise and direct diverse activities in a changing environment, often under time pressure.</li><li>With a mature, self-confident and well-balanced personality, it is essential that the candidate also possess a high standard of ethical and intellectual integrity.</li><li>Finally, the candidate must be strongly computer literate.</li></ul> Click the link below and open the door to the future by submitting your resume today!<li><a href="https://merckgroup.taleo.net/careersection/2/jobdetail.ftl?lang=en&job=0900481" rel="nofollow">EMD Serono 0900481</a></li><div> </div>  <div><img src="http://www.emdserono.com/cmg.emdserono_us/en/images/EMD_Top_employee_tcm115_22986.jpg" height="120" width="180"> <div><div>EMD Serono, Inc. Named as a Top Employer by Science Magazine </div><div></div></div><div><ul><li><a href="http://www.emdserono.com/cmg.emdserono_us/en/images/20081009_en_tcm115_22959.pdf" target="_blank" rel="nofollow">more</a></li></ul></div><div> </div></div> ]]>

<![CDATA[<big></big><center><big>At EMD Serono, Inc. our strength is our people!</big></center>About the CompanyEMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.DescriptionEMD Serono is seeking a well qualified scientist for the Protein Engineering and Monoclonal Antibody Technologies (PEAT) group within New Biological Entities (NBE) Technologies. He/she will head a group of scientists responsible for the development and execution of hybridoma and B cell technologies to support the identification of new antibody therapeutic candidates. This individual will report to the Head of Antibody Technologies at their facility in suburban Billerica, MA and will be part of an energetic team in a key strategic area of the Discovery organization within EMD Serono. This individual will play an important role in delivering target-binding antibodies as well as establishing new antibody discovery capabilities by:<ul><li>Leading a group of two scientists (with the possibility of expansion) in the B cell technology laboratory</li><li>Refining immunization strategies to support antibody discovery for specific and species cross-reactive binders</li><li>Improving hybridoma-based antibody discovery technology</li><li>Establishing technology for individual IgG amplification from FACS-purified non-immortalized single B cells</li><li>Taking responsibility for projects by driving and coordinating his/her direct reports in achieving the specific objectives of the respective research projects.</li><li>Advancing of antibody technologies within his/her own group as well as influencing the strategies on current and future technologies.</li><li>Representing the Protein Engineering and Monoclonal Antibody Technologies Department on specific antibody project teams.</li><li>Responsibility for defining requirements for research projects and identifying potential constraints and risks.</li><li>Evaluating complex issues, and monitoring and initiating corrective actions where necessary.</li><li>Interacting with therapeutic Area scientists for the proposal of new discovery projects.</li></ul>Qualifications<ul><li>The ideal candidate will have a Ph.D. in molecular biology, biochemistry, immunology or biological sciences.</li><li>A strong background is required in molecular biology and B cell technologies (hybridoma as well as SLAM-like technologies). An interest to work part-time at the laboratory bench is desirable.</li><li>Experience with immunization strategies to beak tolerance to generate cross-species binders</li><li>Experience with automation and high throughput implementation</li><li>Familiarity with standard and alternative antibody discovery technologies</li><li>Strong Communication skills-he/she should be confident in presentation with parties both small and large.</li></ul>Click the link below and open the door to the future by submitting your resume today!<li><a href="https://merckgroup.taleo.net/careersection/2/jobdetail.ftl?lang=en&job=1000109" rel="nofollow">EMD Serono 1000109</a></li><div> </div> Awards & RecognitionJune 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work! May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries! October 2008, EMD Serono Named as a Top Employer by Science Magazine!<ul><li><a href="http://www.emdserono.com/en/who_we_are/awards_and_recognition/awards_and_recognition.html" rel="nofollow">more</a></li></ul><div></div><a href="http://www.emdserono.com/en/who_we_are/awards_and_recognition/awards_and_recognition.html/%E2%80%9D%3Emore%3C/a%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv%20class=" rel="nofollow"> </a>]]>

<![CDATA[<big></big><center><big>At EMD Serono, Inc. our strength is our people!</big></center> About the Company EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts. Description<ul><li>To provide scientific regulatory support and expertise to US Regulatory Managers and Directors in terms of source document verification and assessment of publication and report references used for labeling, training, medical and promotional communications.</li><li>Maintain EMD Serono, Inc and relevant affiliates in compliance with government requirements for the import and distribution of products in the US. (e.g., permits, licenses, registrations) and to assist with planning importation of products and resolving import holds. Work closely with the Senior Coordinator, USRA and Global Regulatory Operations, and Senior Director/Head, USRA to ensure establishment and listing compliance.</li><li>Assist with the assessment of compliance with US government requirements with regards to post-approval activities including Medical Information letters, Medical Affairs/Operations field activities, and Commercial activities for marketed products</li><li>Prepare documents, as directed, for FDA submissions related to product labeling updates for safety, new indications, device instructions for use include NDA/SNDA sections, as appropriate for local product life cycle management initiatives</li></ul> KEY TASKS & RESPONSIBILITIES:<ul><li>Provide expertise and support to Supply Chain Department in terms of the management of Homeland Security import requirements for products and declaration preparation in order to facilitate importation of shipments from abroad. Assist with timely release of import holds.</li><li>US Regulatory scientific and technical support for the review of medical and commercial materials used internally and externally (e.g., sales training, speaker programs, sales pieces, etc)</li><li>Conduct data verification of Medical, Marketing, Managed Markets and Sales Training materials vs source documents such as publications, clinical study reports, data on file. Perform limited reviews of proposed claims for compliance with FDA regulations 21CFR202</li><li>Support USRA staff involved in Promotional and Scientific Material Review Meetings by conducting scientific source documentation verification for compliance with 21CFR202. Work with USRA Manager/Director to assess whether support is sufficient for proposed claims. Back-up for Regulatory Managers at PSMR meetings, as requested.</li><li>Assist Sr Director/Head US Regulatory with planning/project management of department activities including Life Cycle Management initiatives lead by US Regulatory. Liaison with Global RA staff to track and update USRA team on status of globally lead submissions for marketed products (e.g., new formulations, strengths).</li><li>Prepare metric reports of USRA importation assists, publication reviews, USDA permit assessments and submissions.</li><li>Write and review SNDA submission content for USRA led submissions with guidance from Sr Director, USRA or designee</li><li>Review pre-publication manuscripts intended to support US business objectives for regulatory concerns. Liasion with publication teams in review and revision of materials, as appropriate.</li><li>Participate in the development and implementation of Regulatory and Market Support Standard Operating procedures (SOPs)</li><li>Prepare and present training programs for speakers, sales and medical science liaisons, field nurses and call center staff</li><li>Special projects as assigned</li></ul>Qualifications EDUCATION/LANGUAGES<ul><li>Advanced Scientific degree (MS, PhD, PharmD</li></ul>PROFESSIONAL SKILLS & EXPERIENCE<ul><li>2- 4 years of expertise in medical/scientific communications for drugs/devices.</li><li>Experience with assessment of scientific quality and rigor of publications and reports.</li><li>Proficient medical/scientific writing skills. Familiarity with FDA and other government regulations regarding drug and device labeling, importation, distribution, and promotion highly desirable.</li><li>Strong attention to detail and quality orientation.</li><li>Project management skills.</li><li>Ability to provide accurate top-level analysis and recommendations for problem-solving. Proficient PC skills (e.g., Word, Excel, PowerPoint, Adobe Acrobat, DataVision).</li></ul> Click the link below and open the door to the future by submitting your resume today!<li><a href="https://merckgroup.taleo.net/careersection/2/jobdetail.ftl?lang=en&job=0901562" rel="nofollow">EMD Serono 0901562</a></li><div> </div> Awards & RecognitionJune 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work! May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries! October 2008, EMD Serono Named as a Top Employer by Science Magazine!<ul><li><a href="http://www.emdserono.com/en/who_we_are/awards_and_recognition/awards_and_recognition.html" rel="nofollow">more</a></li></ul><a href="http://www.emdserono.com/en/who_we_are/awards_and_recognition/awards_and_recognition.html/%E2%80%9D%3Emore%3C/a%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv%20class=" rel="nofollow"> </a>]]>

<![CDATA[<big></big><center><big>At EMD Serono, Inc. our strength is our people!</big></center>About the CompanyEMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.DescriptionProvide laboratory expertise in oncology to support discovery and preclinical projects in the Applied Immunology Research group within TA Oncology. This position focuses on a number of laboratory techniques including (but not limited to) T cell based assays (proliferation, ELISPOT, CTL), ELISA, Flow Cytometry techniques, cancer stem cell isolation/proliferation and in vitro/in vivo mouse work.KEY TASKS & RESPONSIBILITIES<ul><li>The primary responsibilities of this position will be to provide laboratory support, data generation, data analysis, and evaluation/documentation for oncology research for small molecular and/or biological therapeutics in Discovery and pre-clinical development.</li><li>Other tasks involve tailoring assays (if not developing new assays) that projects require in order to push the project forward.</li><li>The candidate will be expected to contribute to studies for multiple projects and present their research in group settings.</li></ul>Specific tasks involve:<ul><li>Performing phenotypic assays in T cells, tumor cells and cancer stem cells for mechanism of action studies, supporting Discovery and Pre-clinical development of lead molecules.</li><li>Designing and implementing immunological assays that can measure immune responses in mouse models and in vitro human PBMC models.</li><li>Using cell-based assays to assess the effects of drug substance alone and in combination with other drug substances.</li><li>Implementation of studies for the identification of biomarkers.</li><li>Data analysis and evaluation.</li></ul>QualificationsEDUCATION & LANGUAGES<ul><li>Bachelors required, Masters an asset</li><li>Must be fluent in both written and spoken English</li></ul>PROFESSIONAL SKILLS & EXPERIENCE<ul><li>Minimum of 2 years experience in a research and/or development environment.</li><li>Immunophenotyping by flow cytometry (FACS).</li><li>T cell isolation, proliferation, cytokine/chemokines and apoptosis assays.</li><li>in vivo mouse cancer models with ability to inject, collect organs and fluids.</li><li>Proficient in mammalian cell culturing and maintenance of cell lines with aseptic techniques.</li><li>Experience with cancer stem cell isolation/culturing desirable.</li><li>Culture and maintenance of mouse embryonic stem (ES) cells desirable.</li><li>High level of computer literacy required, including familiarity with Excel and data analysis software.</li><li>Ability to work independently with input from senior scientists.</li></ul>PERSONAL SKILLS & COMPETENCIES<ul><li>Self-motivated, highly organized, with strong attention to detail.</li><li>Excellent lab, communication, and interpersonal skills.</li><li>Ability work in constantly changing environment and balance working with on multiple projects.</li><li>Ability to change and/or develop entirely new assays as projects demand to continue moving forward.</li><li>Excellent written and oral communication skills are a must.</li><li>Ability to work as part of a team.</li><li>Ability to work at lab bench.</li></ul>Click the link below and open the door to the future by submitting your resume today!<li><a href="https://merckgroup.taleo.net/careersection/2/jobdetail.ftl?lang=en&job=1000139" rel="nofollow">EMD Serono 1000139</a></li><div> </div> Awards & RecognitionJune 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work! May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries! October 2008, EMD Serono Named as a Top Employer by Science Magazine!<ul><li><a href="http://www.emdserono.com/en/who_we_are/awards_and_recognition/awards_and_recognition.html" rel="nofollow">more</a></li></ul><div></div><a href="http://www.emdserono.com/en/who_we_are/awards_and_recognition/awards_and_recognition.html/%E2%80%9D%3Emore%3C/a%3E%3C/li%3E%3C/ul%3E%3C/div%3E%3Cdiv%20class=" rel="nofollow"> </a>]]>

<![CDATA[RF-EME Analyst– Job # 28052 Position Description EBI Consulting is looking to hire a RF-EME Analyst to support a world class blue chip client. We are looking for a leader to support a rapidly growing business into the national market leader. Duties include but not limited to: • Provide RF-EME compliance modeling and safety plan/compliance report review and preparation • Project management for specified clients/portfolios • RF-EME Plan Audit review and development • RF-EME compliance monitoring/field surveys on an as-needed basis. The projects require close attention to detail, experience working with MS-Excel, Word and graphics applications as well as engineering drawings/specifications; specific project experience with wireless facilities and understanding/application of FCC RF-EME guidelines and client RF safety requirements highly desirable. Education Requirements BS in Electrical Engineering, Environmental Engineering, Environmental Science, Safety or equivalent and 2-5 years of experience Company Overview EBI Consulting was founded in 1989 with the purpose of creating value for our clients by utilizing innovative applications of engineering assessments, environmental health and safety (EH&S) management, and due diligence techniques. EBI Consulting is know for the high quality of our product, the professionalism and business expertise of our consultants, our responsiveness, and the personalized nature of our services. EBI Utilizes, and is constantly improving upon, state of the art technology and communications to expedite the delivery of our services. Nationwide offices help to ensure exceptional, efficient, cost-effective and expedited services. EBI has grown and been profitable for more than 20 years, has no indebtedness to banks or outside investors, and is currently investing in new technology and personnel with the primary objective of improving profitability for its clients. EBI’s people have years of successful business and technical management experience with multi-national companies including W.R. Grace & Company, Earth Tech, Dow Chemical’s Rohm & Haas/Shipley Company, and Stone & Webster Engineering. EBI’s personnel have advanced business management and technical degrees including chemistry, biology, geology, geophysics, and structural, civil, electrical and environmental engineering and certified industrial hygiene. For more information about EBI and open positions please visit our website at www.ebiconsulting.com. Plans and Expectations for Future Growth After adjusting to the 2007-2008 changes in economic conditional, EBI has developed and followed an aggressive plan to develop new services and business lines, acquire new clients, and invest in existing lines of business that have the potential for significant growth. Our goal and strategic plan call for EBI to continue to realize substantial revenue increases by providing clients with superior services and providing our employees with training, experiences and career opportunities that enable them to grow and profit from EBI’s growth. What the Successful Candidate should anticipate We expect the successful candidate would work with our team to help EBI realize our goals while at the same time, the successful candidate will realize personal, professional and financial growth. Benefits EBI offers competitive compensation, bonus opportunities, group medical & dental insurance, 401k plan with employer contribution, tuition reimbursement, paid vacation, and progressive career opportunities. EOE M/W/D/V Submittal Please submit a resume and cover letter in Word or PDF format via email to jobs@ebiconsulting.com. You must include the following information: 1. Reference job #, job title and resource 2. Brief summary of past related experience (highlight your experience as it relates to our need & industry); 3. List of your education credentials and professional registrations 4. Salary history We look forward to hearing from you! ]]>