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Director/Associate Director - Regulatory Affairs (United States; Russia; Egypt; Turkey; UAE; Israel; Saudi Arabia) Responsibilities Setting regulatory strategy and translating these strategies into executable plans for specific departments/areas of responsibility Providing2/13/2017 Westborough, MA Save This Job
Description Reporting to the Vice President of Regulatory Affairs, the successful candidate will provide expertise in translating regulatory requirements into practical, workable plans for development stage oncology related drugs and biologics. Candidate will have primary2/4/2017 San Francisco, CA Save This Job
Advertising/Promotion (4582) Req Id 4582 - Posted 03/01/2017 - United States - Massachusetts - Cambridge - Regulatory Affairs ? Job Description Print Preview Apply Apply Using LinkedIn? Save Job Email Job to Friend Return to List Position Summary The Senior Director3/21/2017 Cambridge, MA Save This Job
Tracking Code 307-093 Job Description We are seeking a talented and highly motivated individual to join our team as a Senior Regulatory Affairs Specialist. This position will report directly to the Senior Director, Clinical and Regulatory Affairs. Summary: As a member of the1/25/2017 Lexington, MA Save This Job
SENIOR DIRECTOR, GLOBAL REGULATORY AFFAIRS We have an exciting newly created opportunity for an outstanding Head of Regulatory Affairs in our dynamic, successful and fast growing pharmaceutical company. ABOUT ENANTA Enanta Pharmaceuticals is a research and development-focused2/21/2017 Watertown, MA Save This Job
Sr. Medical Director, Drug Safety (4581) Req Id 4581 - Posted 02/17/2017 - United States - Massachusetts - Cambridge - Pharmacovigilance ? Job Description Print Preview Apply Apply Using LinkedIn? Save Job Email Job to Friend Return to List The Senior Medical3/21/2017 Cambridge, MA Save This Job
Req Id 4561 - Posted 02/03/2017 - United States - Massachusetts - Cambridge - Clinical Operations ? Job Description Print Preview Apply Apply using LinkedIn? Save Job Email Job to Friend Return to List Aegerion Pharmaceuticals, a subsidiary of Novelion Therapeutics,2/19/2017 Cambridge, MA Save This Job
TARIS Biomedical is a unique therapeutically-focused urology company developing drug-device combination products for the treatment of genitourinary diseases. The individual will be responsible for supporting development activities such as analytical method transfer, test method2/15/2017 Lexington, MA Save This Job
Working with CCXI Senior Management, Contract Development Organizations and selected Consultants, this individual is responsible for the development and overseeing the execution of all the technical activities associated with product development in support of Clinical Development1/30/2017 Mountain View, CA Save This Job
Assoc. Director, Clinical Operations? Help Please fill in the information below and use the navigational buttons to continue. Warning: Using your browser's Back and Forward buttons may produce undesirable results. Associate Director, Clinical Operations About Acceleron:1/31/2017 Cambridge, MA Save This Job
Reports to: Vice President, Clinical Development Education: Board certification in Internal Medicine, and preferably additional Board Certification in Pulmonary Medicine or Oncology Job Description This role represents a unique opportunity for a physician experienced in2/22/2017 Boston, MA Save This Job
Req Id 4121 - Posted 11/02/2016 - United States - Massachusetts - Cambridge - Marketing ? Job Description Print Preview Apply Apply using LinkedIn? Save Job Email Job to Friend Return to List Aegerion Pharmaceuticals is a biopharmaceutical company dedicated to the2/19/2017 Cambridge, MA Save This Job
Posted: 9/26/2016 Category: Nuclear Job Type: - Minimum Experience: 4+ years Required Education: Bachelor (BA, BS...) Benefits: - Job Description Position Title: Employee Concerns Program Specialist The Employee Concerns Program Specialist will support the safe operation1/17/2017 New Hill, NC Save This Job