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

Also on the board Same function, level within a rung

Level

Manager

Location

Princeton, NJ

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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