This role is has two key areas of responsibility: 1) support the design, delivery, and continuous refinement of scientific, disease state, product, and capabilities training strategies for Medical Affairs, with a particular focus on ensuring Field Medical colleagues have the knowledge, resources, and materials necessary to communicate accurate, balanced, and scientifically rigorous medical information; and 2) manage the day-to-day Medical Information operations, including responses to unsolicited medical information requests, content strategy, vendor oversight, and adverse event and product quality complaint intake and reporting. The role will partner closely with Medical Affairs, Field Medical, Regulatory, Clinical Development, Safety/Pharmacovigilance, Commercial, Legal, Compliance, and other cross-functional teams to ensure medical information responses, field medical materials, and training content are accurate, compliant, timely, and aligned with approved product information.