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# Senior Manager, Epidemiology/Real-World Data and Analytics (Oncology)

- **Company:** Regeneron
- **Location:** Tarrytown, NY, United States
- **Experience:** Expert
- **Salary:** $150,500.0 - $245,500.0
- **Contract:** Permanent contract
- **Skills:** Clinical Data Repository, Data Analytics
- **Published:** October 18, 2026
- **Apply:** https://www.businessworkforce.com/job.asp?id=3456063099&tx=KK4343FFL&pt=1&aff=0B19D771-A501-4A5E-8338-2A822B784D54&utm_source=Job%20Feed&utm_medium=textkernel&utm_campaign=DE&utm_term=0B19D771-A501-4A5E-8338-2A822B784D54

## About the Role

* Doctoral degree in epidemiology or a related subject area (e.g., health services research, public health), plus at least 2 years of experience across academia, pharma/biotech, or consulting
 * Hands-on experience drafting technical design documents, study protocols and/or statistical analysis plans using real-world data, with a record of peer-reviewed publications
 * Excellent communication skills, with the ability to translate complex designs and findings into clear, actionable insights for diverse audiences
 * Experience conducting epidemiology and RWE research in oncology, including familiarity with cancer treatment paradigms and oncology endpoints is preferred
 * Experience applying advanced analytical methods to large healthcare datasets, including causal inference, bias assessment, and robust estimation is preferred
 * Familiarity with global HTA and payor evidence needs, value and reimbursement strategies are preferred

## Description

* Generate high-quality observational research using diverse real-world data sources to support development and commercial strategies
 * Evaluate and implement emerging design and analytic methods to strengthen our RWE capabilities
 * Synthesize and critically assess scientific evidence for regulatory and payor submissions, press releases, and internal business needs
 * Support global HTA and payor submissions with epidemiology and RWE inputs for value dossiers and reimbursement packages
 * Provide technical expertise to clinical development and evidence generation, and external control arms and hybrid approaches
 * Stay current with evolving regulatory and payor expectations for RWE and guide internal teams on the implications
 * Participate in epidemiologic design discussions in a peer review forum
 * Drive projects forward with a growth mindset, proactively identifying solutions and managing priorities