Associate Director, Medical Affairs (Oncology)

Regeneron Pharmaceuticals • Sleepy Hollow, WY

2d • Onsite

About The Position

As an Associate Director, Medical Affairs Oncology, you will lead the development and execution of our US medical strategy for solid tumors. You will serve as a key scientific and medical resource, providing leadership across evidence generation, external engagement, and internal strategic guidance. A core responsibility is to ensure US medical/clinical activities are aligned with global strategies, goals, and operations driving high-quality, compliant execution. This position is on-site in Sleepy Hollow, NY, 4 days per week. If eligible, we can offer relocation benefits. A remote work option is not available for this role

Requirements

• A doctorate level healthcare degree is required (MD, PharmD, PhD) degree with demonstrated expertise in Oncology (solid tumors) in clinical, research or drug-development.
• A minimum of 6+ years of experience in Medical Affairs required.
• Proven medical communication skills with the ability to tailor complex scientific content to audiences of varying expertise.
• Ability and willingness to travel approximately 40%, including some international travel.

Nice To Haves

• Want to work at the intersection of science, strategy, and patient care.
• Can demonstrate extensive cross-functional collaboration and visibility with senior leaders
• Want an opportunity to shape US medical strategy and influence our direction
• Have the capability to deal with scientific concepts and complexity comfortably.

Responsibilities

• Representing Medical Affairs in cross-functional forums aligning closely with Headquarters Medical Affairs and other functions optimizing strategic and tactical plans.
• Defining and delivering the US tumor area strategy and annual objectives.
• Partnering with Field Medical to translate strategy into action, including scientific exchange and insight generation.
• Providing medical support for our clinical development and research activities, including identifying centers of excellence and key investigators/sites, contributing to investigator meetings, and supporting targeted patient recruitment efforts.
• Leading US scientific engagement with external collaborators advancing appropriate understanding and use of our medicines and improve patient care.
• Developing and implementing US medical strategies for congresses, symposia, advisory boards, and other scientific forums.
• Delivering clear, credible scientific presentations to diverse audiences including physicians, pharmacists, payers and agency partners.
• Providing medical input with scientific integrity into commercialization strategies.
• Leading medical reviewer on the Medical Review Committee (MRC) for review/approval of promotional, educational, and related materials, ensuring accuracy, balance, and compliance.
• Reviewing US Investigator-Initiated Study (IIS) proposals, protocols, and concepts in Medical Affairs Review Committee (MARC) meetings.
• Supporting development and review of US clinical pathways and guideline submissions in partnership with cross-functional teams.
• Translating US insights to inform global strategy; ensure bi-directional communication and alignment with global Medical Affairs and clinical development.
• Managing relevant budgets, timelines, and vendor/agency partners to deliver initiatives on time and within scope.
• Uphold the highest ethical, scientific, and compliance standards across all activities

Benefits

• health and wellness programs (including medical, dental, vision, life, and disability insurance)
• fitness centers
• 401(k) company match
• family support benefits
• equity awards
• annual bonuses
• paid time off
• paid leaves (e.g., military and parental leave)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree