PharmD Clinical Development Fellow

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

Benefits offered by this job

Annual bonuses

Equity awards

Health and retirement benefits

Paid time off

Job summary

Regeneron Pharmaceuticals, Inc. is offering the PharmD Program, a 2-year, interdisciplinary development track for graduating PharmD and PhD candidates. Participants receive mentorship and exposure across global development, with assignments spanning regulatory, clinical, and safety activities.

Location: Tarrytown, NY with up to 15% travel. Responsibilities include drafting regulatory submissions, analyzing clinical data, managing vendors, and developing regulatory strategies to support drug

Qualifications

• Post-doctoral graduates from an ACPE-accredited College of Pharmacy program (PharmD).
• PhD graduates in life sciences may be considered.
• Must complete PharmD and/or PhD by Summer 2027; internship/rotation experience a plus.

Responsibilities

• Drafting documents integral to clinical sites and regulatory submissions.
• Analyzing data from clinical studies for interactions with ethics committees and regulators.
• Managing third-party vendors and maintaining timelines of key results.
• Developing regulatory strategies for clinical development programs.
• Analyzing safety data to characterize product safety profile during development.
• Collaborating with mentors to enhance professional skills.
• Travel to clinical sites or meetings with health authorities.

Skills

Regulatory submissions

Clinical data analysis

Vendor management

Mentorship & coaching

Cross-functional collaboration

Education

PharmD

PhD

Tools

Regulatory tracking systems

Job description

Regeneron Pharmaceuticals, Inc. is offering the PharmD Program, a 2-year, interdisciplinary development track for graduating PharmD and PhD candidates. Participants receive mentorship and exposure across global development, with assignments spanning regulatory, clinical, and safety activities.

Location: Tarrytown, NY with up to 15% travel. Responsibilities include drafting regulatory submissions, analyzing clinical data, managing vendors, and developing regulatory strategies to support drug