Regulatory Affairs jobs in Biotechnology
Broaden your search
Refine your search
-
Biotechnology
Remove selection
-
Regulatory, Regulatory Affairs
Remove selection
- California 25
- Colorado 1
- Illinois 5
- Maryland 10
- Massachusetts 6
- New York 25
- North Carolina 3
- Texas 1
- Washington State 2
- Europe 3
- More…
Found 83 jobs
-
Medical Monitor I
Within Leidos Biomedical Research Inc., the Clinical Monitoring Research Program Directorate (CMRPD) provides high-quality comprehensive and strategic
New
-
Associate Director, Regulatory Affairs
Job Description:Our Associate Director, Regulatory Affairs will be responsible for ensuring all RA deliverables associated with each project or other
New
-
Manager, Regulatory Affairs
Those who join Emergent BioSolutions feel a sense of ownership about their future. You will excel in an environment characterized by respect, innovati
New
-
Senior Manager, Regulatory System Owner, Global Development Systems
The Senior Manager, Regulatory Systems Owner is responsible for leading regulatory systems implementations and operations for the Global Development S
New
-
(Sr) Director, Global Regulatory Strategy
At Intellia, we are revolutionizing medicine by harnessing the power of genome editing to develop potential cures. We bring new hope for people living
-
-
Medical Director
Mirum focuses on finding and developing drugs for difficult to treat liver diseases. Our lead program is focused on two severe liver diseases in child
-
Director, Regulatory Affairs
The Director, Regulatory Affairs is responsible for regulatory affairs for specific drug development programs (pre and post market approval).
-
Director Regulatory/CMC
OVID Therapeutics Ovid Therapeutics (NASDAQ: OVID) is a New York-based biopharmaceutical company using its BoldMedicine™ approach to develop medicines
-
Clinical Operations Lead
This individual leads clinical activity for a first-in-human program and initiates planning for multiple clinical trials currently under development.
-
Clinical Trials Manager
ROLE SUMMARY - CLINICAL TRIAL MANAGER The Clinical Trial Manager (CTM) will oversee multiple multi-site international clinical trials underway at A...
-
VP of Intellectual Property
Lead the intellectual property function of the company, including counselling management on IP matters, overseeing and reviewing preparation and prose
-
Director, Regulatory Affairs CMC
At Retrophin, our mission is to identify, develop and deliver life-changing therapies to people living with rare disease. Giving patients a chance, pr
-
Associate Manager, Regulatory Affairs
The Associate Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects related to
-
Senior Manager, Validation
OverviewReady to join a team committed to developing and commercializing gene therapies for patients and families devastated by rare neurological gene
-
Regulatory Lead, CMC (Associate Director)
The CMC Regulatory Lead will be a key member of the Regulatory Affairs team and interface with various Cell and Gene Therapy groups in the company to
-
Senior Director, Commercial Regulatory (Advertising and Promotion)
Being a part of MyoKardia means you are a pioneer at heart, a go getter, a pa rt of something meaningful. We push the boundaries, embrace uncertainty
-
Director, Regulatory Affairs
At Retrophin, our mission is to identify, develop and deliver life-changing therapies to people living with rare disease. Giving patients a chance, pr
-
Sr Manager, Regulatory Affairs
Those who join Emergent BioSolutions feel a sense of ownership about their future. You will excel in an environment characterized by respect, innovati
-
Associate Director, Program Management
At Intellia, we are revolutionizing medicine by harnessing the power of genome editing to develop potential cures. We bring new hope for people living
-
Director, TMF Management (Contract)
The Director, Trial Master File Management (Contract) will develop and lead a team responsible for management of inspection-ready Clinical Trial essen