PharmD Global Development Program Associate

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

Benefits offered by this job

Annual bonuses

Equity awards

401(k) company match

Job summary

Regeneron is offering a two-year PharmD/PhD development program in its Global Development organization, located in Tarrytown, NY. Associates will gain exposure to Clinical Operations, Regulatory Strategy, and Safety Sciences, with mentorship and rotations across functions.

Candidates must complete PharmD and/or PhD by Summer 2027, with internships or rotations seen as a plus. Up to 15% travel may be required, and onsite work is emphasized.

Qualifications

• Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD).
• PhD graduates within a life science related area of study may also be considered.
• Internship or rotational experience within the Pharmaceutical/Biotech industry a plus
• Exposure or familiarity with evaluating clinical trials, scientific literature and data
• Highly motivated and seek to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences.

Responsibilities

• Drafting documents integral to clinical sites and regulatory submissions.
• Analyzing data from clinical studies in preparation for interactions with ethics committees, senior management, regulatory authorities, and others.
• Managing third-party vendors and maintaining timelines of key results.
• Developing regulatory strategies for clinical development programs.
• Analyzing 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.

Education

PharmD

PhD in life sciences

Job description

Regeneron is offering a two-year PharmD/PhD development program in its Global Development organization, located in Tarrytown, NY. Associates will gain exposure to Clinical Operations, Regulatory Strategy, and Safety Sciences, with mentorship and rotations across functions.

Candidates must complete PharmD and/or PhD by Summer 2027, with internships or rotations seen as a plus. Up to 15% travel may be required, and onsite work is emphasized.