Hybrid Associate Director, Regulatory Project Planning

ACADIA Pharmaceuticals

ACADIA Pharmaceuticals Inc. is seeking an Associate Director for Regulatory Affairs Project Planning & Coordination. This role, based in Princeton, NJ, San Diego, or San Francisco, is crucial for developing and implementing project plans that support the Global Regulatory Affairs department. The ideal candidate will have at least 8 years of regulatory experience in a pharmaceutical setting. This position supports project management and regulatory strategy, with a hybrid work model and competitive salary package, including equity awards and various benefits. #J-18808-Ljbffr

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Vacancy posted 3 hours ago

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