PharmD Global Development Rotational Associate

Regeneron Pharmaceuticals; Village of Tarrytown (NY); On-site; USD 98,000 - 160,000; Full time

Job summary

Regeneron Pharmaceuticals offers a two‑year PharmD Program for graduating PharmD and/or PhD candidates in Regeneron’s Global Development organization. Participants gain depth and breadth through mentors, cross‑functional experiences, and diverse training across clinical operations, regulatory affairs, and safety sciences.

Assignments include trial setup, governance, and integrated drug development planning, with opportunities to travel to clinical sites or meetings with health authorities.

Qualifications

• Post‑doctoral graduates from ACPE‑accredited PharmD program or PhD in life sciences considered.

Responsibilities

• Drafting documents for clinical sites and regulatory submissions.
• Analyzing data from clinical studies for ethics committee and regulatory interactions.
• Managing third‑party vendors and timelines of key results.
• Developing regulatory strategies for clinical development programs.
• Analyzing safety data to characterize product safety across development.
• Collaborating with mentors to reach professional goals and attending cross‑functional meetings.

Education

PharmD

PhD (life sciences)

Job description

Regeneron Pharmaceuticals offers a two‑year PharmD Program for graduating PharmD and/or PhD candidates in Regeneron’s Global Development organization. Participants gain depth and breadth through mentors, cross‑functional experiences, and diverse training across clinical operations, regulatory affairs, and safety sciences.

Assignments include trial setup, governance, and integrated drug development planning, with opportunities to travel to clinical sites or meetings with health authorities.