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Senior Medical Director, Medical Affairs - Rare Disease Team Lead

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

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Role Summary

The Senior Medical Director, Medical Affairs Team Lead leads medical strategies for Regeneron’s Rare Diseases & Cardio-Metabolic franchise, guiding a cross-functional Medical Impact Team in a matrixed environment to align with patient-centric goals and organizational priorities. The role involves development and execution of medical strategies for multiple rare disease assets, shaping the portfolio’s future and serving as a trusted medical and scientific resource internally and externally.

Responsibilities

  • Lead and manage a team of Medical Affairs professionals supporting the General Medicine – Rare Disease Franchise.
  • Develop, oversee, and implement focused medical strategies and tactics for rare disease and cardio-metabolic assets.
  • Drive annual medical planning, scientific communications, and publication strategies.
  • Serve as a key medical and scientific advisor to global and U.S. medical teams, applying disease expertise and business acumen to meet evolving clinical needs.
  • Lead a multifunctional Medical Impact Team (MIT), ensuring seamless collaboration across research, development, commercial, access & reimbursement, and patient advocacy functions.
  • Partner with alliance stakeholders to ensure alignment, consensus building, and efficient decision-making within a matrixed organization.
  • Co-lead the creation and implementation of robust Phase IIIb/IV plans to support pipeline development and lifecycle management.
  • Provide hands-on leadership in the generation and dissemination of high-quality clinical and non-clinical data, driving impactful publications and scientific communications.
  • Oversee the design, execution, and reporting of clinical trials, ensuring timely delivery of high-quality trial documentation.
  • Develop and execute external and internal scientific communication strategies, including presentations and publications.
  • Act as a medical expert in interactions with regulatory authorities, key opinion leaders, advisory boards, healthcare practitioners, research groups, payers, and alliance partners.
  • Build and maintain strategic partnerships with clinical specialists, societies, collaborative groups, advocacy organizations, and other external stakeholders.
  • Represent Regeneron and the franchise at scientific forums, ensuring the company’s values and interests are effectively communicated.

Qualifications

  • Advanced degree (MD, DO, PhD, or PharmD) with strong clinical expertise in Cardiovascular/Metabolics or Rare Diseases.
  • At least 6 years of relevant industry experience, including leadership in medical affairs and successful product launches.
  • Demonstrated expertise in evidence generation, clinical research, and cross-functional team leadership within a matrixed environment.
  • Experience with regulatory filings, health authority interactions, and evidence generation in rare diseases and/or cardio-metabolic diseases.
  • Deep knowledge of compliance and global regulatory requirements.

Skills

  • Medical strategy development and execution
  • Leadership of cross-functional teams
  • Evidence generation and clinical trial oversight
  • Scientific communications and publications
  • Regulatory affairs and health authority collaboration

Education

  • MD, DO, PhD, or PharmD (as above)

Additional Requirements

  • No additional travel or physical demands specified as essential in the provided description.