Medical Director, Medical Affairs

Role Summary

Medical Director, Global Medical Affairs for FOP and Rare Diseases in CVM. Responsible for developing, implementing, and executing medical strategies to support Regeneron’s assets in the rare bone disease space, focusing on Fibrodysplasia Ossificans Progressiva (FOP). Collaborate cross-functionally to ensure ethical, accurate, and customer-focused dissemination of clinical and scientific information aligned with the organization’s strategic objectives.

Responsibilities

• Scientific Expertise & Exchange: Demonstrate expertise in rare diseases such as FOP and rare bone diseases; maintain knowledge of emerging therapies and clinical data; communicate complex information to HCPs, KOLs, and external stakeholders; respond to medical inquiries per guidelines.
• Stakeholder Engagement & Relationship Building: Build and sustain relationships with scientific/medical customers, advocacy groups, and clinical experts; identify and engage KOLs; provide medical education and support at conferences and advisory boards.
• Strategic Collaboration & Cross-functional Partnerships: Collaborate with Medical Affairs, Clinical Development, Medical Operations, HEOR, Publications, and Statistics; share field insights to inform strategy and product development; support promotional material review and training.
• Clinical Trial Support & Data Generation: Support design, conduct, oversight, analysis, and reporting of post-approval FOP trials; attend study team meetings and data reviews; oversee generation and dissemination of data leading to publications.
• Healthcare Trends & Market Access: Assess value/cost of care, hospitalization rates, progression risk, pricing pressures, reimbursement, and market access; provide insights to improve value and appropriate use of Regeneron products.
• Compliance and Governance: Ensure activities comply with legal, regulatory, and company policies.
• Field Leadership & Mentorship: Contribute to projects and field medical training; mentor and support field medical teams as needed.
• This Role May Be For You If You: Are passionate about improving patient outcomes in rare diseases; excel in scientific leadership, communication, and collaboration; are comfortable covering a large geographic territory and engaging with diverse stakeholders.

Qualifications

• MD/DO or equivalent with specialized training in rare diseases.
• Minimum of 3 years of relevant experience (clinical, managed care, or pharmaceutical industry); Medical Affairs or Clinical Development experience strongly preferred.
• Demonstrated expertise in clinical trial execution and scientific exchange.
• Strong presentation and communication skills; ability to deliver succinct, strategic insights to senior management.
• Ability to thrive in a dynamic environment and manage competing priorities.
• Willingness to travel up to 30% and attend national/international conferences as needed.

Skills

• Scientific leadership and communication
• Strategic collaboration and cross-functional teamwork
• Clinical trial design and data interpretation
• Stakeholder engagement and KOL relationships
• Regulatory compliance and governance

Education

• MD/DO or equivalent; specialized training in rare diseases

Additional Requirements

• Willingness to travel up to 30% and participate in national/international conferences as needed.