Director, Content Development

Role: Director, Content Development within Medical Affairs at Acadia Pharmaceuticals, focusing on creating and managing scientific content to support strategic communication and scientific exchange. Responsibilities: oversee development and review of medical materials such as slide decks, congress content, and digital resources; collaborate with cross-functional teams including Corporate Affairs, Investor Relations, and Medical Affairs; evaluate scientific literature, interpret complex data, and ensure accuracy and compliance in all materials; act as a subject matter expert providing timely scientific guidance to internal stakeholders; and manage vendor collaborations. Qualifications: PharmD, PhD, or MD with 7+ years in Medical Affairs and 5+ years in Scientific Communications or Medical Information within the pharma/biotech industry; demonstrated experience in developing medical content supporting scientific exchange activities; strong data interpretation, scientific writing, and regulatory knowledge, especially around MLR and MRC processes. High-Value: focus on neurological and rare disease therapies, including Parkinson’s disease psychosis, Rett syndrome, Alzheimer’s, and Lewy body dementia; supporting late-stage clinical development, regulatory review, and scientific communication. Work setup: not explicitly stated, but involves collaboration with internal teams and external vendors, possibly in a hybrid or remote environment.