Acadia Pharmaceuticals is seeking an Associate Director for Regulatory Affairs Project Planning & Coordination in Princeton, NJ. This role is responsible for developing integrated regulatory project plans and overseeing compliance activities. The ideal candidate should have a Bachelor's degree and at least 8 years of experience in regulatory drug development.
Benefits include competitive compensation, medical insurance, and a hybrid work model. Join Acadia’s mission to innovate in neurological and rare disease treatments.
#J-18808-LjbffrGlobal Regulatory Affairs Project Lead in princeton at Unknown Company
This position is listed as full time and hybrid.