Medical Director, Clinical Development, Endocrinology

Role: Medical Director supporting Regeneron's Endocrinology clinical development, acting as Medical Lead for trials. Responsibilities: guide global clinical study teams, oversee medical monitoring to ensure patient safety and regulatory compliance, lead study and protocol development, and provide scientific input for data review, publications, and stakeholder presentations. Collaborate closely with discovery and cross-functional teams to advance program goals. Requirements: MD with board eligibility or certification in Endocrinology preferred; minimum 2 years pharma or relevant research experience; experience in rare disease drug development is highly advantageous; familiarity with regulatory interactions and CTD submissions is beneficial. HighValue: Endocrinology, rare disease drug development, clinical trial leadership, global stakeholder collaboration, protocol oversight, cross-functional partnership, and experience with regulatory processes. WorkSetup: on-site in Tarrytown, NY, Washington D.C., or Cambridge, MA; travel ~10% for conferences.