PharmD Global Development Program Associate

Regeneron

Village of Tarrytown (NY)

On-site

USD 80,000 - 110,000

Full time

4 days ago

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Job summary

Regeneron seeks candidates for its PharmD Program, an intensive 2-year development track within the Global Development organization. The program blends mentorship with cross-functional project experience in clinical operations, regulatory strategy, and safety sciences.

Based in Tarrytown, NY, participants will rotate through tracks such as Clinical Operations & Program Management, Regulatory Labeling, and Safety Sciences, gaining hands-on work and exposure to ethics committees, regulatory

Qualifications

Post-doctoral graduates from an ACPE PharmD program or PhD in life sciences.
You must have completed your PharmD and/or PhD by Summer 2027.
Internship or rotational experience within the Pharmaceutical/Biotech industry is a plus.
Exposure or familiarity with evaluating clinical trials, scientific literature and data.

Responsibilities

Draft regulatory submissions and clinical site documents.
Analyze clinical study data 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 the safety profile of products throughout their development lifecycle.
Working with program mentors to improve skills to reach professional goals better.
Opportunities to travel to clinical sites and/or meetings with health authorities.