Assoc Dir Health Economics & Outcomes Research, Solid Tumors
Regeneron
June 29, 2026
On-site
Sleepy Hollow, NY
Market Access
Associate Director role developing HEOR strategies and plans, conducting HEOR and RWE studies, and creating publications/deliverables for solid tumors.
Responsibilities:
- Develop and implement global HEOR strategies and programs across the product lifecycle to inform clinical development and regulatory needs and support optimal market access.
- Collaborate to develop compelling product value propositions to optimize future patient access.
- Identify HEOR evidence needs and gaps; design, conduct, and deliver studies/tools for relative value demonstration and product differentiation.
- Use RWD analytic tools and collaborate with HEOR RWDnA and Epidemiology teams to generate insights for development programs and key business questions.
- Co-lead regulatory-grade real-world evidence studies and educate on emerging RWE opportunities across the solid tumor portfolio.
- Conduct and communicate epidemiology and pharmacoepidemiology analyses/studies.
- Provide input on patient population, comparators, and endpoints to demonstrate incremental value over standard of care.
- Develop and implement Clinical Outcomes Assessment (COA) measurement strategies; develop/validate COA endpoints for clinical studies.
- Produce COA evidence dossiers for regulatory submissions.
- Evaluate payer and HTA decisions, gather feedback in advisory meetings, and apply learnings to pipeline products.
- Maintain awareness of regulatory and payer/HTA considerations affecting HEOR program planning.
- Report, publish, and disseminate HEOR data/results in compliance with requirements.
Qualifications:
- Advanced graduate degree (Ph.D., MS, or MD/PharmD; or B.Pharm with Master’s) in an HEOR-related field (e.g., pharmacoepidemiology, epidemiology, healthcare/data analytics, health economics, health services research, public health).
- 4+ years with PhD or 6+ years with MS in HEOR; 3+ years life science company or healthcare consulting experience preferred.
- Strong technical expertise in designing/conducting HEOR studies and models.
- Solid understanding of regulatory (FDA/EMA) and HTA considerations.
- Experience designing/implementing patient experience data in clinical trials (instrument selection, analysis, reporting).
- Oncology experience preferred.
Application:
- Apply now.
Responsibilities:
- Develop and implement global HEOR strategies and programs across the product lifecycle to inform clinical development and regulatory needs and support optimal market access.
- Collaborate to develop compelling product value propositions to optimize future patient access.
- Identify HEOR evidence needs and gaps; design, conduct, and deliver studies/tools for relative value demonstration and product differentiation.
- Use RWD analytic tools and collaborate with HEOR RWDnA and Epidemiology teams to generate insights for development programs and key business questions.
- Co-lead regulatory-grade real-world evidence studies and educate on emerging RWE opportunities across the solid tumor portfolio.
- Conduct and communicate epidemiology and pharmacoepidemiology analyses/studies.
- Provide input on patient population, comparators, and endpoints to demonstrate incremental value over standard of care.
- Develop and implement Clinical Outcomes Assessment (COA) measurement strategies; develop/validate COA endpoints for clinical studies.
- Produce COA evidence dossiers for regulatory submissions.
- Evaluate payer and HTA decisions, gather feedback in advisory meetings, and apply learnings to pipeline products.
- Maintain awareness of regulatory and payer/HTA considerations affecting HEOR program planning.
- Report, publish, and disseminate HEOR data/results in compliance with requirements.
Qualifications:
- Advanced graduate degree (Ph.D., MS, or MD/PharmD; or B.Pharm with Master’s) in an HEOR-related field (e.g., pharmacoepidemiology, epidemiology, healthcare/data analytics, health economics, health services research, public health).
- 4+ years with PhD or 6+ years with MS in HEOR; 3+ years life science company or healthcare consulting experience preferred.
- Strong technical expertise in designing/conducting HEOR studies and models.
- Solid understanding of regulatory (FDA/EMA) and HTA considerations.
- Experience designing/implementing patient experience data in clinical trials (instrument selection, analysis, reporting).
- Oncology experience preferred.
Application:
- Apply now.