Senior Manager, Epidemiology/Real-World Data and Analytics (Oncology)
About The Position
Regeneron is seeking a Senior Manager, Epidemiology for its Health Economics and Outcomes Research team to support Oncology programs. The role generates real-world evidence to influence the development and commercialization of oncology therapies, working with HEOR colleagues and key collaborators. The position is based in Sleepy Hollow, New York, with an on-site work model of four days per week. The Senior Manager will generate and assess observational research using real-world data, apply and evaluate study design and analytic methods, and provide epidemiology and real-world evidence expertise for clinical development, evidence generation, regulatory submissions, health technology assessment, and payer needs. The role also involves communicating scientific findings and guiding internal teams on changing regulatory and payer expectations.
Requirements
- Doctoral degree in epidemiology or a related subject area, such as health services research or public health.
- At least 2 years of experience across academia, pharmaceutical or biotechnology companies, or consulting.
- Hands-on experience drafting technical design documents, study protocols, and/or statistical analysis plans using real-world data.
- Record of peer-reviewed publications.
- Excellent communication skills, including the ability to translate complex study designs and findings into clear, actionable insights for diverse audiences.
Nice To Haves
- Experience conducting epidemiology and real-world evidence research in oncology, including familiarity with cancer treatment paradigms and oncology endpoints.
- Experience applying advanced analytical methods to large healthcare datasets, including causal inference, bias assessment, and robust estimation.
- Familiarity with global health technology assessment and payer evidence needs, value strategies, and reimbursement strategies.
Responsibilities
- Generate high-quality observational research using diverse real-world data sources to support development and commercial strategies.
- Evaluate and implement emerging study design and analytic methods to strengthen real-world evidence capabilities.
- Synthesize and critically assess scientific evidence for regulatory and payer submissions, press releases, and internal business needs.
- Support global health technology assessment and payer submissions with epidemiology and real-world evidence inputs for value dossiers and reimbursement packages.
- Provide technical expertise to clinical development and evidence generation, including external control arms and hybrid approaches.
- Stay current with evolving regulatory and payer expectations for real-world evidence and guide internal teams on their implications.
- Participate in epidemiologic design discussions in a peer review forum.
- Drive projects forward by proactively identifying solutions and managing priorities.
Benefits
- Competitive and comprehensive total rewards package, which may include annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, medical, dental, vision, life and disability insurance, paid time off, and family support benefits.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
Ph.D. or professional degree
