Role Summary
Medical Director, Global Medical Affairs for Fibrodysplasia Ossificans Progressiva (FOP) and Rare Diseases. Leads medical strategies to support Regeneronβs 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
Additional Requirements
- Willingness to travel up to 30% and attend national/international conferences as needed