PharmD Program Associate — Global Development Tracks

Regeneron; Village of Tarrytown (NY); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Travel opportunities up to 15%

Job summary

Regeneron is seeking post‑doctoral graduates (PharmD or PhD) for its 2‑year Global Development rotation program in Tarrytown, NY. The role offers cross‑functional exposure across Clinical Operations, Regulatory Strategy, and Safety Sciences with mentor guidance and multi‑site assignments.

You will draft regulatory documents, analyze clinical data, manage vendors, and develop regulatory strategies while travel to sites and health authorities is possible.

Qualifications

• Post‑doctoral graduates from an ACPE‑accredited College of Pharmacy program (PharmD); PhD in life sciences may be considered.
• Completed PharmD and/or PhD by Summer 2027.
• Internship or rotational experience in Pharma/Biotech is a plus.
• Exposure to evaluating clinical trials, literature and data.
• Motivated to build a career in Clinical Sciences, Global Clinical Operations, Regulatory Affairs or Safety Sciences.
• Eligible to work in the U.S. on a permanent basis.

Responsibilities

• Draft documents integral to clinical sites and regulatory submissions.
• Analyze data from clinical studies for interactions with ethics committees, senior management and regulators.
• Manage third‑party vendors and maintain timelines of key results.
• Develop regulatory strategies for clinical development programs.
• Analyze safety data to characterize product safety across development.
• Collaborate with program mentors to grow professional skills.
• Travel to clinical sites and/or meetings with health authorities.

Education

PharmD or PhD in life sciences

Job description

Regeneron is seeking post‑doctoral graduates (PharmD or PhD) for its 2‑year Global Development rotation program in Tarrytown, NY. The role offers cross‑functional exposure across Clinical Operations, Regulatory Strategy, and Safety Sciences with mentor guidance and multi‑site assignments.

You will draft regulatory documents, analyze clinical data, manage vendors, and develop regulatory strategies while travel to sites and health authorities is possible.