The following career opportunities were posted this week at DNAjobs.com. For each position, I have listed a short description and a link for more information.
As always, I wish you tremendous success in your searching!
Jason
Industrial Post-Doc
(US-Arizona-Phoenix) Ribomed Biotechnologies, Inc. is a Phoenix, Arizona based biotechnology company with a patent pending signal generation technology that we are in the process of applying to the detection of nucleic acids and proteins. [www.ribomed.com] We are currently seaching for an industrial post-doc with expertise in transcription, or other aspects of nucleic acid chemistry for the nucleic acid detection project. We are also seeking several post-docs experienced in antibody assay design, antibody or nucleic acid immobilization, or protein detection for the protein detection project. The company is tripling in size, so we are looking for competent, motivated people who are capable of working independently. Applicants should be ready to conduct experiments and are available to relocate and begin work by the beginning of January, 2004. The laboratory consists of 20,000 square feet of lab space, plus adequate office space for an expanding staff.
(US-Arizona-Phoenix) Ribomed Biotechnologies, Inc. is a Phoenix, Arizona based biotechnology company with a patent pending signal generation technology that we are in the process of applying to the detection of nucleic acids and proteins. [www.ribomed.com] We are currently looking for lab technicians experienced in antibody assay design, antibody or nucleic acid immobilization, or protein detection who will not require a great deal of training, but are ready to conduct experiments and are available to begin work by the beginning of January, 2004. Applicant must have at minimum one years relevant experince in a laboratory that is listed as a primary reference. The company is tripling in size, so we are looking for competent, motivated people who are capable of working independently. Applicants should be ready to conduct experiments and are available to relocate and begin work by the beginning of January, 2004. The laboratory consists of 20,000 square feet of lab space, plus adequate office space for an expanding staff.
(US-Illinois) Our client, a major pharmaceutical company in Lake County, IL is looking for a Analytical Scientist, Pharmaceutical Dev. - B with the following qualifications: REQUIRES 3-5 YEARS EXPERIENCE Analytical function with the Pharmaceutical Development department plans, executes and supports all activities related to the testing of bulk drug substance, drug product, intermediates, raw materials, excipients, commodities and/or any other component which is critical to the therapeutic performance of the final product. Analytical Scientist supports this function within the department under considerable supervision of senior staff. BS Preferred. EDUCATION B.S or M.S. in cell biology, biochemistry or related field. EXPERIENCE B.S. with at least 3-6 years in pharmaceutical industry or related lab experience, or M.S. with at least 0-3 years experience in assisting in the discovery or development of drugs / drug candidates. Broad background in cell biology or biochemistry with specific experience in tissue culture and / or biochemical techniques, such as cell-based assays, SDS-PAGE and Western blotting.
(US-Illinois) Our client, a major pharmaceutical company in Lake County, IL is looking for a Clinical Data Coordinator - A with the following qualifications: REQUIRES 0-3 YEARS EXPERIENCE Experienced data management professional who is responsible for all activities relating to over 20 studies over the course of 1 year. The primary goals are to provide accurate data acquisition and to furnish accurate and well-documented study databases to the statistical and clinical teams. Also includes Case Report Forms; initiating the purchase of CRFs, diaries, and related documents from clinical protocols, preparing the study database dictionary; developing quality assurance database checks. BS Preferred. Perform data management tasks on clinical studies as work experience increases. This may include, but is not limited to CRF design, database dictionary design, quality plan creation and study documentation activities. Candidate should have the following Oracle Clinical database experience: data entry, Discrepancy Management, DCF creation and printing, and report creation using SQL.
(US-Illinois) Our client, a major pharmaceutical company in Lake Forest, IL is looking for a Clinical Research Professional II - B with the following qualifications: REQUIRES 3-5 YEARS EXPERIENCE Experienced in the finer details of the Clinical Trial process. More directly or indirectly involved through review meetings, and by actively participating in study audits by the Sponsor Company and/or FDA inspectors. Prepare information for NDA sections and/or IND submissions, including reports on data information generated from Phase I - IV studies. Experience of 1 - 5 years in Biotechnology and/or Clinical Research Industry. Salt Lake City, UT -- 1 Field Monitor needed. **BS required** Nursing Background/BSN preferred. Minimum of 1 year experience in field monitoring. Preferred experience in monitoring studies in the following therapeutic areas: Gastrointestinal, rheumatology, urology, or oncology, women's health. Laptops will be provided to field monitors.
(US-New Jersey) PharmD or MS Required. New positions, any type therapeutic experience but cardio or CNS would be a plus. Prefers local candidates but will consider relo. Director is responsible for all review and approval for symposiums, articles, labeling with RA, CT info, promotional approval process, and must deal with internal and external vendors. This person will have the oppty to make medical presentations and attend seminars on behalf of the company and the products.
(US-Missouri-Kansas City/Independence) Our client, a major pharmaceutical company in Kansas City, MO is looking for a Clinical Research Professional II - B with the following qualifications: REQUIRES 3-5 YEARS EXPERIENCE Experienced in the finer details of the Clinical Trial process. More directly or indirectly involved through review meetings, and by actively participating in study audits by the Sponsor Company and/or FDA inspectors. Prepare information for NDA sections and/or IND submissions, including reports on data information generated from Phase I - IV studies. Experience of 1 - 5 years in Biotechnology and/or Clinical Research Industry. Kansas City, MO -- 1 Field Monitor needed. **BS required** Nursing Background/BSN preferred. Minimum of 1 year experience in field monitoring. Preferred experience in monitoring studies in the following therapeutic areas: Gastrointestinal, rheumatology, urology, or oncology, women's health. Laptops will be provided to field monitors. Position will likely be extended past the projected end date.
(US-New York-Westchester) This is an entry level position. The individual should have experience in formulation chemistry including the hands on experience in analytical methods such as TLC, HPLC, IR, NMR, DSC, microscopy, light scattering, drug dissolution, and x-ray diffraction. The individual should also have a working knowledge of drug solubilization and the surfactants and lipids used as excipients in formulation and drug delivery is highly desired. BS or MS in Chemistry or Pharmaceutical Sciences with 1-3 years of research/industrial experience in formulations and drug delivery.
(US-Massachusetts-Western/Springfield) Responsible for global communication and correspondence with the company’s clients, including pharmaceutical research units and academic research laboratories. Responsible for development, implementation and maintenance of client management systems, relating to inquiry tracking and management. A key management position, reporting to the President.
