PharmD Rotational Program Associate - Regulatory Labeling

Regeneron; Village of Tarrytown (NY); On-site; USD 70,000 - 95,000; Full time

Job summary

Regeneron is seeking graduates for a 2-year PharmD/PhD development program in Tarrytown, NY. The role offers cross-functional rotations across Clinical Operations, Regulatory Strategy, and Safety Sciences, with mentorship and exposure to global development processes.

Participants will draft regulatory documents, analyze clinical data, manage vendors, and develop strategies for clinical programs while traveling to sites and health authorities as needed.

Qualifications

• Post-doctoral graduates from an ACPE PharmD program or PhD in life sciences may be considered.
• You must have completed your PharmD and/or PhD by Summer 2027.
• Prior internship or rotational experience in pharma/biotech is a plus.
• Exposure to evaluating clinical trials, scientific literature and data is expected.
• Motivation to build a career in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences.
• Eligible to work in the U.S. on a permanent basis.

Responsibilities

• Draft documents for clinical sites and regulatory submissions.
• Analyze data from clinical studies for interactions with ethics committees and regulatory authorities.
• Manage third-party vendors and maintain timelines.
• Develop regulatory strategies for clinical development programs.
• Analyze safety data to characterize product safety across development lifecycle.
• Collaborate with mentors to reach professional goals and participate in travel to clinical sites or health authority meetings.

Skills

Clinical data analysis

Regulatory knowledge

Project coordination

Cross-functional collaboration

Education

PharmD

PhD in life sciences

Job description

Regeneron is seeking graduates for a 2-year PharmD/PhD development program in Tarrytown, NY. The role offers cross-functional rotations across Clinical Operations, Regulatory Strategy, and Safety Sciences, with mentorship and exposure to global development processes.

Participants will draft regulatory documents, analyze clinical data, manage vendors, and develop strategies for clinical programs while traveling to sites and health authorities as needed.