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Manager, Regulatory Affairs
**PRIOR PHARMACEUTICAL AND REGULATORY AFFAIRS EXPERIENCE A MUST!!**
• Coordination, preparation and review of regulatory submissions (INDs/NDAs)
• IND/NDA maintenance ...
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Product Development Engineer
Product Development Engineer (expired)Sort By
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LocationJob TitleCompanyDateWayne, NJ...
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Quality Assurance Engineer
Under the general direction of the Vice President of Quality Assurance & Regulatory Affairs, is responsible for quality planning and implementation relating to design ...
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Specialist, Government Contracts - Fed
Sanofi-Synthelabo and Aventis Pharmaceuticals, part of the sanofi-aventis Group are facing the future and leading the way as the 3rd largest pharmaceutical company in ...
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Account Manager
Position Summary:
The Account Manager (AM) is responsible for leading and delivering on project deliverables for Client(s), as well as identifying new business ...
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International Clinical Trial Manager (ICTM), in Oncology
Sanofi-Synthelabo and Aventis Pharmaceuticals, part of the sanofi-aventis Group are facing the future and leading the way as the 3rd largest pharmaceutical company in ...
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Regulatory Affaird Associate Director
Baxter International Inc., assists healthcare professionals and their patients with the treatment of complex medical conditions, including cancer, hemophilia, immune ...
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Sr. Research Investigator
Sanofi-Synthelabo and Aventis Pharmaceuticals, part of the sanofi-aventis Group are facing the future and leading the way as the 3rd largest pharmaceutical company in ...
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Clinical Trials Mgr
The Clinical Trials Program Manager is responsible for program facilitation and management support to the Clinical Program Leader and research team. The Program Manager ...
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Medical Writer needed for contract at pharma co in Bloomsbury, N
Kelly Clinical Resources is seeking a Medical Writer for a pharmaceutical company in Bloomsbury, NJ.
This is a 6 month contract.
This position will be based within the ...
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