Job Opportunities API

The Public Ledger of Openings

← Back to the ledger

Regulatory Programs Lead — Global Submissions & Planning

Acadia Pharmaceuticals Inc.
CompanyAcadia Pharmaceuticals Inc.
CategoryLegal & Compliance
LocationSouth San Francisco
RemoteOn-site (inferred)
EmploymentNot stated
LevelLead
SalaryNot stated by the employer
Posted9 Aug 2026
Last verified12 Aug 2026
SourceThe employer's own careers page (company_site)
Applications are handled by the employer, not by us.Apply on the employer's 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