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Job description
Senior Director, Patient Advocacy
Role Summary: The Senior Director, Patient Advocacy leads Regeneron's disease area enterprise-wide advocacy strategy and operating model, integrating the patient voice across the continuum of discovery, development, and commercialization. This leader exercises independent judgment in ambiguous environments, influences executive decision-making, and builds scalable processes that elevate patient impact, operational efficiency, and company reputation. The role serves as a trusted advisor to senior leadership and a visible ambassador to advocacy and professional organizations.
Location and Work Model
This role is based in Sleep Hollow, NY, 4 days/week.
Impact and Scope
Develops the overarching patient advocacy strategy across multiple therapeutic areas, with enterprise visibility and executive engagement
Establishes standard methodologies and governance for engagement with advocacy and professional societies
Advises cross-functional contributors in Medical, Commercial, Market Access, Policy, and Clinical Development with view to multi-year roadmap on advocacy strategy
Accountable for measurable improvements in disease awareness, time to diagnosis, clinical trial awareness, access, and patient experience
Operates at both strategic and operational level; drives outcomes through cross-functional leadership
Roles and Responsibilities
Strategy and Leadership
Define and evolve the disease area patient advocacy strategy, translating corporate objectives into a prioritized, outcome-based portfolio
Standardize engagement frameworks, decision rights, and operating mechanisms that scale across therapeutic areas and regions
Anticipate external trends and policy shifts as well as shifting company priorities to frame and be comfortable and strategic about recommending tactical choices and trade-offs with clear implications for patients and the business
Help establish governance and operating mechanisms that support alignment, speed and accountability across department
Advocacy Strategy and Execution
Create and maintain therapeutic area strategies and operating plans, including educational programs, disease awareness, advisory boards, patient speaker engagement, clinical trial awareness, and coordination on relevant policy initiatives
Support development and deployment of advocacy campaigns; ensure external partner plans align to Regeneron's goals and compliance standards
Define and report outcome-based KPIs; implement dashboards to monitor reach, quality, and ROI of advocacy efforts
Executive Engagement and Influence
Serve as a trusted advisor to senior executives; deliver board-ready materials that articulate patient impact, risks, and investment options
Lead executive forums and steering committees to drive aligned decisions across competing priorities
Relationship Management
Lead relationship development with key patient advocacy and professional societies to build durable, mission-aligned partnerships
Ensure Regeneron's leadership position is evident through presence at priority events; synthesize and disseminate insights to internal stakeholders
Cross-Functional Collaboration and Alignment
Build strong, collaborative relationships with Medical, Commercial/Brand, Market Access, Government Affairs, Health Policy, Clinical Development, and Legal/Compliance
Drive cross-functional alignment (including at top senior leadership levels, e.g. VP level) and execution of advocacy initiatives; co-create plans with Alliance partners where applicable
Contribute to departmental strategy, annual planning, budgeting, and digital portal development
Patient Voice and Insights
Systematically capture and translate patient insights to inform clinical trial design, evidence generation, disease education, patient services, and access strategies
Champion a patient-centric mindset and embed patient perspectives in enterprise decisions and roadmaps
Financial and Business Acumen
Own budgeting and optimize for impact
Grants and Governance
Strategically fund programs that advance patient engagement and disease education aligned to therapeutic priorities
Oversee transparent, compliant grant review processes; manage budgets and financial stewardship effectively and in a timely manner
Qualifications Required
Bachelors degree and 12+ years of industry experience, including 10-15+ years in Patient Advocacy leading multi-stakeholder programs
Demonstrated enterprise thinking with a track record of cross-functional visibility, influence and company-wide impact
Executive presence with superior communication skills; able to craft concise, data-driven narratives and board-ready materials
Proven operational rigor: building repeatable processes, governance, and metrics with measurable outcomes, experience collaborating with Medical, Commercial, Market Access, and Policy partners; strong familiarity with compliance in advocacy contexts
Preferred
Experience in rare diseases, oncology, hematology, ophthalmology, immunology, and/or cardio-metabolic
Background operating in complex, matrixed, or global environments; alliance management experience
Reporting and Collaboration
Reporting Line
Reports to Executive Director, Patient Advocacy; may manage direct report(s)
Key Internal Partnerships
Up to SVPs across Medical, Commercial, Market Access, Government Affairs, and Health Policy embedded in the business
Salary
$216,100.00 - $360,200.00 annually
Equal Opportunity Employer Statement
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.