Regulatory Programs Lead — Global Submissions & Planning
Acadia Pharmaceuticals Inc.
| Company | Acadia Pharmaceuticals Inc. |
| Category | Uncategorised |
| Location | South San Francisco |
| Remote | On-site (inferred) |
| Employment | Not stated |
| Level | Not stated |
| Salary | Not stated by the employer |
| Posted | 9 Aug 2026 |
| Last verified | 12 Aug 2026 |
| Source | The employer's own careers page (company_site) |
Description
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.
#J-18808-Ljbffr