Director, Global CMC Regulatory Affairs
acadia pharmaceuticalsPrinceton, NJ
Director, Global CMC Regulatory Affairs
acadia pharmaceuticalsPrinceton, NJ
yesterday
Industries
Pharmaceutical Preparation ManufacturingResearch and Development in Biotechnology (except Nanobiotechnology)Biological Product (except Diagnostic) ManufacturingAbout the role
Acadia Pharmaceuticals seeks a Director, Regulatory CMC to lead global regulatory CMC strategies from development through commercialization. You will guide cross-functional teams, interact with regulatory authorities, and shape development and lifecycle plans for worldwide programs.
This role focuses on small molecule therapies and requires extensive regulatory submission experience. The position involves travel and a hybrid work model, with office days in Princeton, NJ, or other US locations as
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JOB OVERVIEW
Experience level
Manager
Location
Princeton, NJ
Occupation
Regulatory Affairs Managers
Industry
Pharmaceutical Preparation Manufacturing
Posted
yesterday
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