Senior Medical Director - MASH - Medical Affairs

Role Summary

Senior Medical Director, Medical Affairs – MASH Assets, will lead medical strategy and execution for MASH assets, reporting to the VP, Medical Affairs, General Medicine. Responsible for strategic planning, cross-functional leadership, and external engagement to ensure medical affairs activities are scientifically rigorous and patient-centric.

Responsibilities

• Provides visionary leadership in the development, execution, and refinement of medical strategy and tactics for assigned assets, aligning with corporate and global objectives; integrates scientific communications, publications, annual medical planning, and field communication strategies with stakeholders.
• Apply therapeutic area expertise to proactively identify and address evolving medical needs in clinical practice; ensure appropriate use of investigational medicines and anticipate trends affecting patient care, policy, and access.
• Directs generation, management, and dissemination of robust clinical and non-clinical data; drives publication strategies and ensures content supports medical strategy and stakeholder needs with scientific rigor.
• Leads cross-functional and cross-alliance teams to ensure strategic alignment, collaboration, and execution excellence; fosters innovation and accountability across medical, commercial, regulatory, and alliance partners.
• Serves as a strategic advisor on global and US cross-functional teams, providing authoritative scientific and medical perspectives to inform strategy and decision-making.
• Oversee design, conduct, and reporting of Medical Affairs studies, ensuring scientific integrity, regulatory compliance, and alignment with priorities; provide mentorship to teams executing these initiatives.
• Cultivates long-term partnerships with clinical experts, societies, advocacy organizations, payers, policy makers, and other external stakeholders; acts as primary ambassador for Regeneron in the MASH therapeutic area.
• Leads prioritization and support for investigator-initiated studies; participates in internal Scientific Review Committees to ensure alignment with medical strategy and objectives.
• Oversees and ensures scientific accuracy and compliance of all medical materials, including promotional and non-promotional content; provides final approval to uphold scientific and ethical integrity.

Qualifications

• Must have an MD or MD equivalent
• 5 years of related industry experience in global or US medical affairs
• Solid background in drug development and life-cycle management
• Experience with working in an alliance setting strongly preferred
• Ability to lead technical and business discussions and explain scientific/medical concepts to all levels
• Ability to cultivate and maintain relationships with leading medical/scientific experts
• Ability to establish trust through demonstrated scientific expertise and follow-through with key opinion leaders
• Strong leadership and management skills
• Attention to detail in analyses, deliverables, and communications
• Strong presentation and communication skills; ability to provide succinct, strategic insights to senior management
• Proactive self-starter who can lead work and manage others independently
• Ability to juggle multiple projects
• Thorough understanding of the healthcare environment and external stakeholders

Skills

• Strategic medical leadership
• Medical affairs strategy and execution
• Data generation, management, and publication planning
• Clinical and non-clinical data analysis
• Cross-functional collaboration and alliance management
• Scientific communication and stakeholder engagement
• Regulatory and compliance awareness
• Investigator-initiated studies oversight
• Editorial and content approval processes

Education

• MD or MD equivalent required

Additional Requirements

• Thorough understanding of the healthcare landscape and external stakeholders