Director, Medical Content Strategy

Acadia Pharmaceuticals; San Diego (CA); On-site; USD 191,000 - 239,000; Full time

Benefits offered by this job

Medical insurance

401(k) plan with company match

Stock Purchase Plan

Paid vacations

Job summary

Acadia Pharmaceuticals is seeking a Director, Content Development to lead medical content creation and scientific review across Medical Affairs. You will partner with stakeholders to ensure accurate, timely scientific information related to Acadia’s products and therapeutic areas, guiding materials used in scientific exchanges.

You will oversee review processes with MLR/MRC, provide expert medical guidance, and help communicate evolving clinical data to support informed decision-making and

Qualifications

• PharmD, PhD, or MD in a scientific discipline or related field is required.
• 7+ years of Medical Affairs experience in pharma/biotech.
• 5+ years in Scientific Communications, Medical Information, or related medical content functions.
• Experience developing medical content to support scientific exchange activities.
• Experience with MLR and MRC review processes.
• Strong ability to interpret scientific data and translate into clear communications.

Responsibilities

• Oversee development of medical content for scientific exchange (slides, booth content, digital materials).
• Coordinate with stakeholders to develop medical content management plans.
• Review corporate, investor relations, commercial, and medical materials for scientific accuracy.
• Provide medical guidance to MLR/MRC teams and manage external vendors.

Education

PharmD, PhD, or MD in a scientific discipline or related field

Tools

MLR/MRC review processes

Job description

Acadia Pharmaceuticals is seeking a Director, Content Development to lead medical content creation and scientific review across Medical Affairs. You will partner with stakeholders to ensure accurate, timely scientific information related to Acadia’s products and therapeutic areas, guiding materials used in scientific exchanges.

You will oversee review processes with MLR/MRC, provide expert medical guidance, and help communicate evolving clinical data to support informed decision-making and