DNAjobs.com is proud to feature the following jobs posted May 15 - 22 (listed in chronological order). 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
Technical Leader / Product Development
(US-Georgia-Atlanta) Champion and execute development of household products that grow Business Units’ sales and profits. Serve as a Technical Leader within the group and within T&I. Develop cutting-edge technology Foster technical excellence in others. Develop new products and new product area concepts. Manage, maintain and oversee team operations and activities appropriately to provide customers (internal and external) with on-time objective accomplishment while striving for operational excellence.
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Molecular Biologist
(India-Bangalore) An established MNC involved in Genomic Research require Team Leader-M.sc or PHD in Life sciences with experience in DNA synthesis and should be able to lead a team of 4 to 5 scientists.
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Program Director / Professor of Bioinformatics
(US-Oklahoma) Minimum Education and Experience: Masters Degree in Bioinformatics or associated fields (Biology, Biotechnology, Chemistry, Biochemistry, Mathematics or Information Technology) with significant work experience in bioinformatics. A minimum of 18 graduate credit hours in the Masters Degree field is required. Preferences Teaching experience at the post-secondary level, with emphasis on community college experience. Familiarity with competency based education.
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Post-Doctoral Positions
(Canada) We are seeking capable, highly motivated individuals to fill 1 or 2 post-doctoral positions at Norgen Biotek. The positions will be supported by industrial NSERC scholarships for up to three (3) years. Applicants must have a recent Ph.D. in the last 5 years to qualify. Applicants with expertise in mammalian viruses, cell culture, gene transfer, and DNA cloning are preferred.
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Medical Director
(US-Massachusetts) Our client, a biotechnology company in the Boston area, is leading the way in research, development and the manufacture of pharmaceuticals to combat alcohol addiction. Join this innovative team as the Medical Director and provide guidance and leadership in the development and commercilization of these products.
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Sales Manager
(US-Texas-Houston) The Sales Manager is responsible for developing, motivating and evaluating the performance of Inside Sales representatives to insure all sales growth and revenue goals are met. Also responsible for defining sales opportunities abd communitcating commission plans, marketing intiatives and sales goals to group. Will also be responsible for customer service.
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Head Analytical Chemistry
(France) The candidate has to be able to quickly understand the needs and problems of a small, dynamic start-up company. He/she will work independently, but in close collaboration with the medicinal chemistry team, develop analytical methods to measure purity of compounds and implement operationally the analytical facilities. We require several years of experience in the analysis of pharmaceutical compounds, excellent knowledge of instrumental techniques, good knowledge of GLP and GMP.
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Senior Medical Writer
(US-Pennsylvania-Philadelphia) We are searching for a talented writer to be responsible for researching, writing and editing medical manuscripts, white papers, abstracts, slide kits and scientific posters in a wide range of therapeutic areas. As a writer you will be a member of dedicated client teams and have direct interaction with clients and physicians in developing medical communications.
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Pharmacist
(France) To coordinate the pharmaceutical development of our new compounds we are looking for a pharmacist with extraordinary organizational skills. In collaboration with external and internal experts you organize and coordinate pre-formulation and formulation studies, and actively participate in the preparation of materials for clinical trials.
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Pre-Clinical/Clinical Project Manager Psychiatry
(France) We are looking for a MD, eventually Ph.D. with a profound interest in drug discovery and development. We expect the candidate to have deep knowledge/experience in pre-clinical and clinical pharmacology of schizophrenia, anxiety and depression. The candidate will be given responsibility for compounds in pre-clinical and clinical development stage.
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Senior Laboratory Automation Leader / Manager
(New Jersey) Assume responsibility for all aspects of managing and running the laboratory in high-throughput and high accuracy performance mode. Experience of 5+ years running high-throughput assays using automated and robotic systems (not necessarily SNPs or genomics); hands on optimizing and trouble-shooting complex chemical assays; work well in a team environment; highly accurate and productive work track record is essential.
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Marketing Manager, CV Products
(US-Michigan) Develop new product and annual marketing plans, product promotional strategies, advertising programs and new marketing/sales materials. Evaluate results and administer expenses. Develop and present new product launch. Write technical communication for field and distributor sales force. Conduct market and competitive research. Analyze product performance with regulatory, technical support and QC Personnel.
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Marketing Manager, Medical Device Products
(US-California) Provide the company with sales forecasts, product training, marketing communications, technical clinical communications and new product supplier development. Develop and present new product launch. Develop new product and annual marketing plans and new marketing/sales materials. Write technical communications for field and distributor sales force. Conduct market and competitive research.
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Postdoc Position
(US-New York) One postdoc position is available immediately for recent NIH funded project on stem cell research and tissue engineering. Candidates should be familiar with molecular biology and cell biology and highly motivated for success. Salary is competitive and negotiable.
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Ph.D. Fellowships - 14 Positions
(Germany) The Max-Planck-Institute for Plant Breeding Research together with the University of Cologne, the Institute of Bioorganic Chemistry (Poznan, Poland), the Institute for Plant Sciences (Gif sur Yvette, France) and the Biological Research Centre (Szeged, Hungary) invite applications for 14 Ph.D. fellowships. The ADOPT program is intended for highly motivated students with a strong training in molecular sciences.
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Research Associate
(US-Pennsylvania) Seeking responsible person to perform experiments in molecular and cell biology. Successful candidate will have knowledge and experience in basic molecular biology techniques including cloning, restriction analysis, PCR and plasmid preparation. In addition, experience in tissue culture systems(sterile eukaryotic cell handling and maintenance, transfection techniques, and reporter protein analysis) is desirable.
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Clinical Project Leader (Manager) - 3 Positions
(US) We have an exciting opportunity for 3 qualified Project Leaders to join a leading international clinical research organization. This position will provide a leadership role in managing multiple Phase I-IV clinical trials in a variety of therapeutic areas. The Clinical Project Leader will report to and work closely with the Group Leader (Director) to ensure the client's goals are met.
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Senior Clinical Research Associate
(US-California-Silicon Valley/San Jose) Reporting to the Clinical Operations Manager, you will manage clinical trials for the ranolazine program and lead the development and support of study-specific metrics. Responsibilities include overseeing activities associated with multiple clinical studies in accordance with designated project assignments; ensuring compliance with FDA regulations and ICH guidelines; and designing study documents, including clinical protocols, case report forms, site study manuals and project tools.
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Manager / Sr. Manager Regulatory Affairs
(US-California-Silicon Valley/San Jose) This position will serve as the Regulatory Affairs representative on one or more project teams (ranolazine, tecadenoson), providing regulatory support for development which may include nonclinical, clinical, manufacturing (CMC), and marketing issues. In addition, this position will manage the preparation, review and assembly of regulatory filings, such as IND filings and amendments, marketing applications and supplements.
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Senior Quality Assurance Associate
(US-California-San Francisco) Assist in vendor qualification activities and vendor auditing for drug and device. Perform internal auditing of systems and records. Assist in facilitating, maintaining and improving client’s Quality System for device and drug compliance to appropriate laws, regulations, and government standards. Write SOPs to improve Quality System operations. Provide initial assessment of discrepancies, initiate, investigate, follow-up and complete process for handling significant quality events.
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Senior Regulatory Affairs Specialist
(US-California-Silicon Valley/San Jose) Responsibilities: 1. Represent Regulatory Affairs Department at project development meetings. 2. Form regulatory assessment for project release. 3. Prepares 510(k), Letters to File, IDE, PMA?s and their supplements for FDA review and approval. 4. Assists in preparation, review and approval of Document Change Orders, especially those concerning device labeling and package inserts.
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Quality Assurance Auditor
(US-California-San Francisco) This client offers central radiology service dedicated exclusively to clinical trials. Their in-house radiologists and scientists are leading authorities in the use of medical imaging and molecular markers in drug development, and have pioneered many methods currently used in clinical trials. Job Duties: Perform database audits of interim/final data transfers. Perform study-specific and Departmental internal audits.
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Clinical Project Manager
(US-California-San Francisco) Lead multi-discipline project teams in delivery of clinical trial services to sponsors. Responsibilities: Lead project team of radiology, densitometry, molecular markers, data management, engineering and science. Manage study activities, direct and coordinate efforts across client's offices for the delivery of services and multiple data sets.
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Manager, Statistical Programming
(US-California-Silicon Valley/San Jose) In this position you will lead statistical programming activities in one or more clinical projects, directly reporting to the head of analytical programming group. You will set up programming standards for the project; develop, maintain, and validate statistical programs. Lead programming for ISS, ISE and electronic regulatory submissions in assigned clinical project.
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PhD Studentship
(Switzerland) The successful candidate will use a combination of molecular and cell biology approaches, including RNA inhibition (RNAi) to study receptor tyrosine kinase signalling in AML cells, with a particular emphasis on phosphoinositide 3-kinases and their role in tumor cell proliferation and resistance to chemotherapy.
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