PharmD Program Associate - Clinical Sciences
Regeneron
August 24, 2026
On-site
Tarrytown, NY
Clinical Research and Development
Responsibilities:
- Draft documents integral to clinical sites and regulatory submissions
- Analyze data from clinical studies for interactions with ethics committees, senior management, regulatory authorities, and others
- Manage third-party vendors and maintain timelines of key results
- Develop regulatory strategies for clinical development programs
- Analyze safety data to characterize product safety profiles throughout the development lifecycle
- Work with program mentors to improve skills toward professional goals
- Travel to clinical sites and/or meetings with health authorities (up to 15%)
Qualifications:
- Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD); PhD graduates in a life science related area may also be considered
- PharmD and/or PhD completed by Summer 2027
- Exposure or familiarity with evaluating clinical trials, scientific literature, and data
- Prior internship or rotational experience in the Pharmaceutical/Biotech industry (plus)
- Eligible to work in the U.S. on a permanent basis
Skills/Focus:
- High motivation to build a career foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences
Application Instructions:
- Submit a resume and cover letter specifying the track of interest; if applying to more than one track, rank preferences
- Applications accepted: August 24, 2026 – September 11, 2026
- Draft documents integral to clinical sites and regulatory submissions
- Analyze data from clinical studies for interactions with ethics committees, senior management, regulatory authorities, and others
- Manage third-party vendors and maintain timelines of key results
- Develop regulatory strategies for clinical development programs
- Analyze safety data to characterize product safety profiles throughout the development lifecycle
- Work with program mentors to improve skills toward professional goals
- Travel to clinical sites and/or meetings with health authorities (up to 15%)
Qualifications:
- Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD); PhD graduates in a life science related area may also be considered
- PharmD and/or PhD completed by Summer 2027
- Exposure or familiarity with evaluating clinical trials, scientific literature, and data
- Prior internship or rotational experience in the Pharmaceutical/Biotech industry (plus)
- Eligible to work in the U.S. on a permanent basis
Skills/Focus:
- High motivation to build a career foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences
Application Instructions:
- Submit a resume and cover letter specifying the track of interest; if applying to more than one track, rank preferences
- Applications accepted: August 24, 2026 – September 11, 2026