Regulatory Programs Lead — Global Submissions & Planning

Acadia Pharmaceuticals is seeking an Associate Director for Regulatory Affairs Project Planning & Coordination. This role involves developing and implementing project plans, ensuring regulatory strategy execution, and overseeing regulatory submissions both pre- and post-approval.

Candidates should have a minimum of 8 years in regulatory development within the pharmaceutical industry and a relevant bachelor’s degree. The work is hybrid, requiring three days in the office per week.