This individual will work closely with the Director, Medical Information, Medical Affairs, Clinical Development, Regulatory, Pharmacovigilance, Commercial, and external vendors to ensure consistent, high-quality scientific exchange, while tailoring medical information content and processes to the condition, stage of development, and stakeholder needs. Reporting to the Director, Medical Information, this role will serve as a hands-on content and operational lead, responsible for the development, review, and maintenance of high-quality, accurate, and compliant medical information delivered to internal and external stakeholders.