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<![CDATA[Seeking a Medical Research Technologist to support the Infectious Diseases Clinical Research Program (IDCRP) at Fort Benning, GA. A highly qualified candidate for the position has extensive clinical microbiology experience and is skilled in the identification and characterization of multi-drug resistant organism. The IDCRP is a collaborative research effort with the National Institute of Allergy and Infectious Diseases (NIAID). Established at USUHS in 2005, this unique program aims to strengthen infectious disease clinical research in the U.S. It brings together a network of clinical scientists at military treatment facilities who are focused on conducting patient-based research on a wide range of infectious diseases relevant to the military and the broader medical communities. RESPONSIBILITIES: 1. Performs microbiological identification procedures including microscopic techniques, culture methods, and phenotypic and molecular methods. 2. Prepares and maintains laboratory manuals as required by the College of American Pathologists (CAP). Submit all manuals for necessary review and approval. 3. Prepares and maintains diagnostic reagents. Maintain an adequate stock of reagents for clinical and research programs. Appropriate records will also be maintained in an organized manner. 4. Maintains stored and working cultures of organisms used in the laboratory. 5. Organizes and maintains a specimen repository and executes specimen pulls, growths, and shipping for future research studies. 6. Provides proper preventive maintenance, calibration, operation and quality control of laboratory instruments and equipment necessary to obtain an accurate determination of laboratory procedure. 7. Recognizes any abnormal results obtained and promptly bring this information to the attention of the Chief of the Service or supervisor. 8. Coordinates with study collaborators to addresses supply problems and issues related to sample labeling and receipt. 9. Coordinates with the data analysts overseeing the study information to resolve questions. 10. Assists research staff with prospective and retrospective research projects including collection, case report form completion and organization of data. 11. Participates in the design and development of research protocols, developing, evaluating, modifying, and/or adopting new methods or revising standard techniques to improve accuracy, precision, sensitivity, specificity, or proficiency of test analysis. Advises investigators of research capabilities, workload, etc. to assist in the design of protocols. 12. Provides other support, as needed, to infectious disease diagnostic and research programs. Required Knowledge, Skills, and Abilities: Professional knowledge of microbiology technology principles, concepts and methodology applicable to a wide range of duties, and a high level of skill in applying that knowledge to solve complex problems concerning a broad range of tests, procedures and protocols. Knowledge of computer applications sufficient to enter, maintain and manipulate data in a database. Experience in planning and organizing work to make optimal use of available time and resources in a busy clinical setting. Extensive experience with sample labeling, packing, marking and transport to meet IATA requirements for Biological Substance, Category B. General knowledge of laboratory medicine with specific knowledge of methods related to isolation and identification of MRSA, including use of selective media, identification schema, susceptibility testing and molecular methods for detection of the mecA gene. Knowledge of molecular epidemiology techniques such as PCR and pulse field gel electrophoresis (PFGE). Knowledge in electronic databases for collection of clinical microbiology results (CHCS, AHLTA) Minimum Education/Training Requirements: Bachelor’s or Master’s degree in related scientific field. Minimum Experience: 4-6 years Work Environment: Laboratory environment Please apply on-line at www.hjf.org/careers Click “Advanced Search” and enter job number 205123 in the Job Opening ID box. OR fax your resume to 240-314-7334. Please specify title and job number on fax. HJF is a nonprofit medical research organization that provides support services to the military medical community and offers a competitive salary and generous benefits package. AA/EEO For a comprehensive list of our benefits, please visit: <a href="http://www.hjf.org/careers/benefits.html" rel="nofollow">http://www.hjf.org/careers/benefits.html</a> HJF administers innovative medical research, supports education and training, and facilitates collaborations between the military and private medical communities. We provide comprehensive management and scientific services for more than 1,000 basic, clinical and applied research projects conducted around the globe. We also support continuing medical education programs for more than 160 military medical research and treatment facilities, and military medical organizations. ]]>

<![CDATA[Grifols has been a leader in the healthcare industry since 1940 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols' activities focus on fulfilling the needs of its patients as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 60 years, Grifols has developed, manufactured and marketed product designed to improve human health. At its Los Angeles facility, Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. For more information, please visit our website: <a href="http://www.grifolsusa.com/" rel="nofollow">http://www.grifolsusa.com/</a> ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. <ul> <li>Adhere to corporate compliance in all activities, including those related to clinical studies, scientific presentations, and responses to unsolicited requests for information.</li> <li>Maintain clinical, scientific, and technical expertise in specific therapeutic areas:  attend relevant symposiums, scientific workshops, key technical meeting and preceptorships; review key scientific journals</li> <li>Represent the Medical Affairs Department to the clinical investigator community</li> <li>Identify, establish and maintain long-term collaborative relationships with key opinion leaders and institutions strategic to product development</li> <li>Develop and maintain collaborative relationships with current and future industry leaders to identify scientific communication opportunities including abstract and manuscript publication, and Continuing Medical Education (CME) sponsorship </li> <li>Upon request , provide scientific/clinical information at advisory board meetings </li> <li>Respond to and document unsolicited requests for off-label information on our marketed products or products in clinical development</li> <li>Represent company products at medical information exhibits during scientific symposiaUpon request, provide support for scientific content development and/or scientific review of content and presentation materials</li> <li>Participate in medical education for healthcare professionals through presentations at investigator meetings, advisory boards, and other appropriate venues to enhance product knowledge</li> <li>Upon request, provide product appropriate medical/scientific support for the sales force </li> <li>Provide internal clinical training at Commercial functions </li> <li>Requires approximately 60-70% travel </li> <li>Territory Includes: OH, KY, TN, AR, LA, MS, AL, GA, FL, SC, NC, VA, WV, Washington DC</li> </ul> Required Skills: <ul> <li>Good computer skills including proficiency with Microsoft Word, PowerPoint, and Excel.</li> <li>Demonstrated high quality interpersonal and communication skills including presentation skills</li> <li>Strong analytical, conceptual and administrative skills.</li> <li>A proven ability to work independently as well as in cross functional networks.</li> <li>High sense of urgency and commitment to excellence in the successful achievement of objectives.</li> </ul> Experience Required: <ul> <li>Advanced Clinical/Science degree required (MD, PhD, PharmD)</li> <li>Minimum 2-3 years MSL experience, or clinical experience in relevant medical discipline </li> </ul> Please apply online at: <a href="http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=217212&company_id=16052&jobboardid=550" rel="nofollow">http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=217212&company_id=16052&jobboardid=550</a>]]>

<![CDATA[The Henry M. Jackson Foundation (HJF) is seeking a Clinical Research Coordinator for the Infectious Disease Clinical Research Program (IDCRP) in Fort Benning, GA. HJF provides scientific, technical and programmatic support services to IDCRP. Responsibilities are to perform clinical research and patient treatment in conjunction with one or more specified clinical research protocols. Incumbent will be supervised by either Clinical Site Manager or designee. The IDCRP is a collaborative research effort with the National Institute of Allergy and Infectious Diseases (NIAID). Established at USUHS in 2005, this unique program aims to strengthen infectious disease clinical research in the U.S. It brings together a network of clinical scientists at military treatment facilities who are focused on conducting patient-based research on a wide range of infectious diseases relevant to the military and the broader medical communities. Responsibilities: 1. Interviews patients for protocols and collects and analyzes appropriate data for recruitment purposes, determine patient commitment and obtains informed consent. 2. Reviews new patient records and screens patients for eligibility for participating in research protocol. 3. Assists to administer appropriate drugs/devices/infusions to patients as specified in protocols. Draws blood (if trained) and obtain other specimens as specified in protocols. 4. Educates patients about the research protocol, their roles in the protocols, and any other vital information and acts as a research case manager for the patients where appropriate. 5. Assists research team to identify problems in the research design or analysis methodology and trends in patient reactions to treatment. 6. Collects, organizes, catalogs, disseminates, and maintains appropriate files of current data. 7. Determines whether data is clinically significant and reports results that warrant prompt action to the physicians. 8. Maintains weekly/monthly status reports on all patients. 9. Acts as a liaison between patients and physicians and serves as a resource for the patients. 10. Prepares and maintains manual and computerized data in patient study books according to prescribed standards. 11. Transcribes and resolves queries of data in case report forms (hardcopy or electronic) and prepares documents, under direction of project heads, reporting statistical analyses and descriptive data from patient's study books to be used in research reports. 12. Adheres to legal, professional and ethical codes with respect to confidentiality and privacy. Assures that protocol requirements are achieved within Good Clinical Practice. 13. Assists with monitoring audits/visits for protocols. 14. Locally travels to/from their assigned workplace to support protocols as needed. 15. Schedules patients for appointments and visits. 16. Performs other duties as needed. Required Knowledge, Skills, and Abilities: Knowledge of federal and local regulations and policies pertinent to research involving human subjects; excellent interpersonal and computer skills; ability to communicate effectively and to work with individuals of all levels Minimum Education/Training Requirements: Bachelor's degree in a scientific discipline preferred. Minimum Experience: 0 to 2 years experience working with research protocols Physical Capabilities: Long periods of sitting and standing; some bending, lifting, and walking; escorting patients and carrying light items; may encounter patients who are confused, agitated, or abusive Required Licenses, Certification or Registration: Certified as a Clinical Research Coordinator (CCRC), Clinical Research Professional (CCRP) and/or Clinical Research Associate (CCRA) preferred; certified in basic cardiac life support preferred. Work Environment: Laboratory, office or clinical/hospital environment; possible evening and/or weekend hours. Please apply on-line at www.hjf.org/careers Click “Advanced Search” and enter job number 205122 in the Job Opening ID box. OR fax your resume to 240-314-7334. Please specify title and job number on fax. HJF is a nonprofit medical research organization that provides support services to the military medical community and offers a competitive salary and generous benefits package. AA/EEO For a comprehensive list of our benefits, please visit: <a href="http://www.hjf.org/careers/benefits.html" rel="nofollow">http://www.hjf.org/careers/benefits.html</a> HJF administers innovative medical research, supports education and training, and facilitates collaborations between the military and private medical communities. We provide comprehensive management and scientific services for more than 1,000 basic, clinical and applied research projects conducted around the globe. We also support continuing medical education programs for more than 160 military medical research and treatment facilities, and military medical organizations. ]]>

<![CDATA[We currently have one opening for Wet Chemistry and Instrumental Analysis Laboratory Technician Duties : Tests and analyzes in-process product (bulk), finished products and samples according to protocol. Provides support to raw material testing. Writes reports and fills out QC forms completely. Submits all completed forms to QC Supervisor for final approval and release. Prepares and standardizes test solution and reagents. Maintains supplies necessary for designated area. Calibrates lab instruments. Maintains cleanliness and good housekeeping in work area including proper disposal of waste products. This is a full-time, hourly position, infrequent overtime may be required. Applicants must have Chemical sciences background. A successful candidate must be able to work in a fast paced environment, work well with others, work efficiently with minimal supervision and have a positive attitude. To be considered for this position, please reply via e-mail with a current cover letter, resume, and (optional) salary history and requirements.]]>

<![CDATA[Our client currently is looking for a lab technician with microbiology experience to monitor cultures for the presence of microbial growth. The following will be the primary job functions for this position: -Read cultures for the presence / absence of microbial growth -Update computer and reports negative cultures -Spin blood to separate serum / plasma from cells -Receive incoming materials -Transfer organisms -Perform routine QC -Determine breaks in aseptic technique -Determine if QC parameters have been met -Other duties may include: -Performing the duties of a general lab technician -Environmental monitoring -Sampling water systems -Bioburden testing -Studies as assigned Required Skill set: -Bachelors degree in Microbiology or 2 year degree & 2 years exp in a related field -Organized, detail-oriented, able to follow instructions. Written records must be accurate. -Good verbal communications skills required. -Capable of working without direct supervision -Works well with others The position is a temporary 3 month contract. The work schedule will be Friday, Saturday, and Sunday from 7am to 7:30pm. ]]>

<![CDATA[Environmental Chemist with a minimum of 5 years experience needed immediately. Candidate must possess all of the following work experience for consideration: GC/MS and ICP/MS analysis of environmental samples, proven experience working with a LIMS system and CLP work, and the ability to work well in busy lab as a member of a team of chemists. Please submit resume, cover letter and salary expectation for immediate consideration. ]]>

<![CDATA[Full time position for a marine aquarium technician with a stable and growing company. Responsibilities include, but not limited to, aquarium maintenance, livestock acclimation, treatment and quarantine. Marine Biology background preferred. Please email resume or CV and salary requirements. Emails without the requested information will not be considered. ]]>

<![CDATA[Medical Device company looking for qualified candidate. Hours are first shift. Duties and Responsibilities: * Monitoring of work performed to assure SOPs and Work Instructions are being followed * Assuring Batch Records are filled out accurately and that no problems or adverse trends are being encountered * Participate in internal investigations and complaint investigations * Proactively provide solutions to collagen production process * Participate in internal and external audits * Write and update work instructions and batch records as needed * Is the technical content expert for the collagen production process and performs troubleshooting and implements solutions to production problems * Maintains clean and sanitary conditions in the work area and provides technical inputs associated with micorbial controls and monitoring Education and Experience: * BS in science, Chemistry preferred * 2-5 years of experience in manufacturing, medical device preferred * Working knowledge of lab equipment such as centrifuges, glassware washers and sterilizers, refrigerators, freezers, and mixers * Knowledge of and experience with biological and temperature sensitive processes * Knowledge of Solid Works, Excel, PowerPoint, Word, and data backup systems * Strong team player Work Environment: * Clean Room * Air conditioned office space * No unusual physical activities required]]>

<![CDATA[A leading environmental laboratory is seeking a Field Service Technician. The qualified candidate will work mainly outdoors monitoring groundwater, surface water, air, soil, and waste water samples.This person will collect and perform on-site testing of the samples using a variety of equipment, create and maintain data records for state and local permits, and monitor sites for major clients throughout the southeast. They must be detailed oriented, able to complete task in a timely manner, and take initiative to better our growing department. Overnight travel approximately 40-60% Flexible schedule: typically between 6:00 AM to 6:00 PM Compensation will be increased based on previous experience. Qualifications BS in Environmental Sciences or related fields mandatory 40hr OSHA Certification Current and applicable computer skills necessary Valid drivers licenses without major moving violations Must be able to work outdoors through out the year in all weather conditions Occasional lifting (up to 60 lbs.) required Submit Resume and list of References ]]>

<![CDATA[Inviragen, Inc. is an international biotechnology company headquartered in Fort Collins, Colorado with offices in Madison, Wisconsin and Singapore that develops vaccines for emerging infectious diseases. Over 15 million people worldwide die each year of infectious diseases; vaccines to prevent these diseases are one of the most cost effective means of improving global health. Inviragen’s vaccines will take advantage of new trends in the global vaccine marketplace including the growing economies of developing countries, new global vaccine initiatives and increasing public and government awareness of the value of vaccines. Inviragen has three products poised to begin human clinical testing: vaccines to protect against dengue fever, hand, foot, and mouth disease (HFMD) and Japanese encephalitis. Inviragen is also developing vaccines to protect against chikungunya, West Nile, human papillomavirus, influenza and a combination vaccine to protect against both plague and smallpox for biodefense. The company is currently recruiting a full-time Postdoctoral Scientist/Scientist to work on Inviragen`s influenza vaccine project in the Madison Wisconsin facility. Essential Duties and Responsibilities: • Designing and conducting animal studies to determine the safety and efficacy of novel influenza vaccines • Assessing the immunological nature of the protective immune responses generated by Inviragen`s candidate vaccines • Tabulating, recording, analyzing and graphing data for meetings, presentations and manuscripts • Interacting with vaccine development teams and coordinating activities with other team members • Participating in drafting grant proposals of vaccine research and development • Drafting and completing manuscripts describing results of Inviragen`s viral vaccine research The ideal candidate will have the following qualifications: • PhD in virology, molecular virology or immunology • Experience in influenza virological and immunological techniques • Experience in small animal experimentation • Publication record in the field of virology, immunology, vaccine research or related field. Papers on influenza will be an asset • Experience working in BSL3 lab facility • Selected agent clearance would be an asset • Project management ability to plan and successfully execute animal studies within timelines • Excellent oral and written communication skills Inviragen offers a competitive salary and an excellent benefits package. Please apply asap for position to start in March. To apply, send cover letter, resume/CV and three references to: Human Resources Inviragen, Inc. hr@inviragen.com ]]>

<![CDATA[TRUTECH, INC WILDLIFE REMOVAL TECHNICIAN (Atlanta, GA) COMPANY PROFILE We have stood the Tru test of time with a long history of quality services and a high standard of professionalism. Incorporated in 1984, and our president has been in the industry for five decades. Trutech provides wildlife removal and pest control service in Alabama, Florida, Georgia, North Carolina, South Carolina, Tennessee and Texas. Leading pest control companies, universities and numerous county and state agencies routinely recommend our services. Trutech provides solutions for all of your WILDLIFE and PEST control problems. JOB DESCRIPTION Perform Wildlife and Animal Removal services for residential and commercial properties. Perform conflict resolution between the public and nuisance wildlife. Perform minor repair work for clients to prevent future wildlife problems. Contact interested individuals by phone to discuss the resolution options available to them. Maintain your own schedule to service clients on a daily basis. Reasons to choose Trutech for your career: â€¢ Exciting and Rewarding Hands-on Career â€¢ Substantial Earning Potential â€¢ Excellent benefit package to include outstanding medical, dental and vision plans, paid time-off and 401k â€¢ Company vehicle provided. Company pays for all gas and vehicle service â€“ cut down your commuting costs! â€¢ Rapidly growing company with numerous advancement opportunities. REQUIREMENTS This is an exciting career opportunity for a select few. We prefer to train candidates with education in one of the following areas: Biology Animal Sciences Entomology Business Or experience in the following areas: Pest Control Hunting/Trapping Sales/Customer service Additional Requirements: Excellent Communication Skills Self-Motivated Enthusiastic Enjoy finding creative solutions Strong Desire to Succeed Enjoy Dealing with Animals and Insects Enjoy Challenges Ability to Work Independently Physically Fit Ability to Carry & Climb 32â€™ Ladder Not Afraid of: Heights (Roof) Confined Spaces (Attic/Crawl Space) Water (Lakes, Streams, Rivers) Not Allergic to Insect Stings Good Driving Record HOW TO APPLY Email your resume to Marilyn Bradley, Human Resources Manager, at mbradley@trutechinc.com ]]>