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Medical Director, Medical Affairs

Regeneron
Remote friendly (Sleepy Hollow, NY)
United States
Medical Affairs

Role Summary

Medical Director, Global Medical Affairs for Fibrodysplasia Ossificans Progressiva (FOP) and Rare Diseases. Leads medical strategies to support Regeneron’s assets in the rare bone disease space, with cross-functional collaboration to ensure ethical, accurate, and impactful dissemination of clinical and scientific information aligned with company objectives.

Responsibilities

  • Demonstrate expertise in rare diseases such as FOP and other rare bone diseases, and monitor emerging therapies and competitive landscape
  • Communicate complex scientific and clinical information to HCPs, KOLs, and external stakeholders
  • Respond to medical inquiries with integrity and regulatory compliance
  • Build and sustain relationships with scientific/medical customers, advocacy organizations, and clinical experts
  • Identify and engage KOLs and decision makers in the rare bone disease community
  • Provide medical education and support at conferences, symposia, and advisory boards
  • Collaborate with internal teams to ensure coordinated activities and share actionable field insights for strategic planning
  • Support commercial activities, including promotional material review, and training
  • Support design, conduct, oversight, analysis, and reporting of post-approval FOP clinical trials
  • Attend clinical study team meetings and work with CRO monitors to support PI and site engagements
  • Oversee generation and dissemination of clinical and non-clinical data leading to high-quality publications
  • Assess value/cost of care, reimbursement, market access, and provide insights to improve product value
  • Ensure all activities comply with legal, regulatory, and company policies
  • Contribute to field medical training programs and mentor field medical teams

Qualifications

  • Required: MD/DO or equivalent with specialized training and experience in rare diseases; minimum 3 years of relevant experience (clinical, managed care, or pharmaceutical industry)
  • Preferred: Experience in Medical Affairs or Clinical Development; demonstrated expertise in clinical trial execution and scientific exchange
  • Strong presentation and communication skills; ability to deliver succinct, strategic, actionable 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 collaboration
  • Clinical trial design, execution, and data interpretation
  • Medical education and stakeholder engagement
  • Strategic thinking and cross-functional partnership

Education

  • MD or DO or equivalent

Additional Requirements

  • Willingness to travel up to 30% and attend national/international conferences as needed