Senior Medical Director - MASH - Medical Affairs

Regeneron Pharmaceuticals•Warren, MI

24d

About The Position

The Senior Medical Director, Medical Affairs – MASH Assets, will play a pivotal and highly visible strategic leadership role within the organization, reporting directly to the VP, Medical Affairs, General Medicine. This role is responsible for driving the medical strategy and execution for MASH assets, with a strong focus on strategic planning, cross-functional leadership, and external engagement. The Senior Medical Director will ensure all medical affairs activities are delivered with scientific excellence, integrity, and patient-centricity. A typical day in this role might look like: Provides visionary leadership in the development, execution, and continuous refinement of medical strategy and tactics for assigned assets, ensuring alignment with corporate and global objectives. Champions the integration of scientific communications, publications, annual medical planning, and field communication strategies in partnership with key internal and external stakeholders. Apply deep therapeutic area expertise and strategic business acumen to proactively identify and address evolving medical needs in clinical practice. Ensures the medically appropriate use of investigational medicines and anticipates future trends impacting patient care, policy, and access. Directs and oversees the generation, management, and dissemination of robust clinical and non-clinical data. Drives high-impact publication strategies and ensures scientific content supports both the medical strategy and external stakeholder needs, maintaining the highest standards of accuracy and scientific rigor. Leads cross-functional and cross-alliance teams with a focus on strategic alignment, collaboration, and excellence in execution. Fosters a culture of innovation and accountability, ensuring seamless coordination across medical, commercial, regulatory, and alliance partners. Serves as a key strategic advisor and leader on global and US cross-functional teams, providing authoritative scientific and medical perspectives that inform and shape organizational strategy and decision-making. Oversee the design, conduct, and reporting of Medical Affairs studies, ensuring scientific integrity, regulatory compliance, and alignment with strategic priorities. Provides mentorship and guidance to teams executing these initiatives. Cultivates and expands long-term, strategic partnerships with clinical experts, societies, collaborative groups, advocacy organizations, payers, policy makers, and other external stakeholders. Acts as the primary ambassador for Regeneron, building trust and advancing shared goals in the MASH therapeutic area. Leads prioritization and support for investigator-initiated studies, serving as a key decision-maker and member of internal Scientific Review Committees. Ensuring alignment with overall medical strategy and organizational objectives. Overseas and ensures the scientific accuracy and compliance of all medical materials, including promotional and non-promotional content. Provides final approval and guidance to uphold the highest standards of scientific and ethical integrity.

Requirements

Must have an MD or MD equivalent
5 years of related industry experience in global or US medical affairs
Solid background and experience in drug development and life-cycle management
Ability to lead technical and business discussions internally and externally and explain scientific/medical concepts to all levels
Ability to cultivate and maintain relationships with leading medical/scientific experts in the relevant fields
Ability to establish trust through the consistent demonstration of scientific expertise and satisfactory follow-through on requests from key opinion leaders
Strong leadership and management skills
Attention to detail in analyses, deliverables, and communications
Strong presentation and communication skills; must be able to provide succinct, strategic, and actionable insights to senior management
A proactive self-starter who can lead work and manage others independently, with the ability to see the next step and take actions without prompting
Ability to juggle multiple projects
Thorough understanding of the healthcare environment including all external stakeholders

Nice To Haves

Experience with working in an alliance setting strongly preferred

Responsibilities

Provides visionary leadership in the development, execution, and continuous refinement of medical strategy and tactics for assigned assets, ensuring alignment with corporate and global objectives.
Champions the integration of scientific communications, publications, annual medical planning, and field communication strategies in partnership with key internal and external stakeholders.
Apply deep therapeutic area expertise and strategic business acumen to proactively identify and address evolving medical needs in clinical practice.
Ensures the medically appropriate use of investigational medicines and anticipates future trends impacting patient care, policy, and access.
Directs and oversees the generation, management, and dissemination of robust clinical and non-clinical data.
Drives high-impact publication strategies and ensures scientific content supports both the medical strategy and external stakeholder needs, maintaining the highest standards of accuracy and scientific rigor.
Leads cross-functional and cross-alliance teams with a focus on strategic alignment, collaboration, and excellence in execution.
Fosters a culture of innovation and accountability, ensuring seamless coordination across medical, commercial, regulatory, and alliance partners.
Serves as a key strategic advisor and leader on global and US cross-functional teams, providing authoritative scientific and medical perspectives that inform and shape organizational strategy and decision-making.
Oversee the design, conduct, and reporting of Medical Affairs studies, ensuring scientific integrity, regulatory compliance, and alignment with strategic priorities. Provides mentorship and guidance to teams executing these initiatives.
Cultivates and expands long-term, strategic partnerships with clinical experts, societies, collaborative groups, advocacy organizations, payers, policy makers, and other external stakeholders. Acts as the primary ambassador for Regeneron, building trust and advancing shared goals in the MASH therapeutic area.
Leads prioritization and support for investigator-initiated studies, serving as a key decision-maker and member of internal Scientific Review Committees. Ensuring alignment with overall medical strategy and organizational objectives.
Overseas and ensures the scientific accuracy and compliance of all medical materials, including promotional and non-promotional content. Provides final approval and guidance to uphold the highest standards of scientific and ethical integrity.

Benefits

We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

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