PharmD Program Associate - Regulatory Strategy
Regeneron
August 24, 2026
On-site
Tarrytown, NY
Corporate Functions
Location: Tarrytown, NY. Travel: up to 15%.
Regulatory Strategy (Regulatory Associate) — Support global regulatory planning and execution for clinical development, approval, and lifecycle management of pharmaceutical products; partner cross-functionally to define regulatory pathways, ensure compliance with global health authority requirements and guidance, and produce/manage timelines and deliverables across multiple programs; provide strategic input on regulatory operations and submissions.
Discover Your Role:
- Draft documents for clinical sites and regulatory submissions
- Analyze data from clinical studies for ethics committees, senior management, regulators, and others
- Manage third-party vendors and maintain timelines for key results
- Develop regulatory strategies for clinical development programs
- Analyze safety data to characterize product safety profile across development
- Work with program mentors to improve skills and reach professional goals
- Opportunities to travel to clinical sites and/or meetings with health authorities
This Role Requires:
- PharmD graduates from an ACPE-accredited College of Pharmacy; PhD graduates in a life science area may be considered
- PharmD and/or PhD completed by Summer 2027
- Prior internship or rotational experience in Pharmaceutical/Biotech (plus)
- Exposure/familiarity evaluating clinical trials, scientific literature, and data
- Highly motivated to build a career foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences
- Eligible to work in the U.S. on a permanent basis
Application Details:
- Include resume and cover letter specifying the track; rank tracks if applying to more than one
- Applications Accepted: Aug 24, 2026–Sep 11, 2026
Salary Range (annually): $98,100.00–$160,100.00
Regulatory Strategy (Regulatory Associate) — Support global regulatory planning and execution for clinical development, approval, and lifecycle management of pharmaceutical products; partner cross-functionally to define regulatory pathways, ensure compliance with global health authority requirements and guidance, and produce/manage timelines and deliverables across multiple programs; provide strategic input on regulatory operations and submissions.
Discover Your Role:
- Draft documents for clinical sites and regulatory submissions
- Analyze data from clinical studies for ethics committees, senior management, regulators, and others
- Manage third-party vendors and maintain timelines for key results
- Develop regulatory strategies for clinical development programs
- Analyze safety data to characterize product safety profile across development
- Work with program mentors to improve skills and reach professional goals
- Opportunities to travel to clinical sites and/or meetings with health authorities
This Role Requires:
- PharmD graduates from an ACPE-accredited College of Pharmacy; PhD graduates in a life science area may be considered
- PharmD and/or PhD completed by Summer 2027
- Prior internship or rotational experience in Pharmaceutical/Biotech (plus)
- Exposure/familiarity evaluating clinical trials, scientific literature, and data
- Highly motivated to build a career foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences
- Eligible to work in the U.S. on a permanent basis
Application Details:
- Include resume and cover letter specifying the track; rank tracks if applying to more than one
- Applications Accepted: Aug 24, 2026–Sep 11, 2026
Salary Range (annually): $98,100.00–$160,100.00