Director, Content Development

Role: Lead the development and scientific review of medical content within Medical Affairs, supporting strategic communication and scientific exchange for Acadia's neurological and rare disease programs. Responsibilities: oversee creation and review of slide decks, congress materials, and medical information resources; collaborate with internal teams (including Corporate Affairs, Investor Relations, Commercial); interpret complex scientific data; ensure accuracy and compliance; serve as a subject matter expert on product knowledge, disease states, and literature; communicate emerging scientific insights to stakeholders. Requirements: PharmD, PhD, or MD; 7+ years in Medical Affairs within pharma/biotech; 5+ years in Scientific Communications or Medical Information; experience with scientific data interpretation, literature evaluation, and regulatory review processes; strong analytical and communication skills. HighValue: focus on underserved neurological and rare diseases, supporting mid- to late-stage clinical programs, with an emphasis on scientific exchange activities. WorkSetup: not specified, but involves regular collaboration with cross-functional teams and external vendors; travel details not provided.