2027 Summer Intern Clinical Trial Operations & Study Start-up
About The Position
Regeneron is seeking multiple 2027 interns to support its Clinical Trial Operations teams. These teams plan and run clinical studies, including starting up sites, coordinating with research organizations and vendors, and tracking progress to help trials stay on schedule. Interns will contribute to a fast-growing, science-driven organization focused on developing medicines for people with serious diseases. The internship is full-time and onsite in Armonk, NY; Warren, NJ; or Tarrytown, NY, from May or June through August. Work may include supporting study start-up activities; coordinating with contract research organizations (CROs) and vendors; maintaining trackers and metrics; managing study documents; capturing lessons learned across drug programs; and assessing study feasibility and potential trial sites. The work involves coordination, Excel use, document management, and communication with study teams, with attention to compliance details. One project is better suited to a graduate student. Relevant academic programs include Pharmacy (PharmD), Biology, Chemistry, Biomedical Engineering, Statistics/Data Science, and Computer Science/Information Technology. Interns must be enrolled in or accepted to an undergraduate or graduate academic program, and must be returning to school the semester following the position or graduating after it. Demonstrated leadership and a cumulative GPA of 3.0 or higher are preferred.
Requirements
- Must be enrolled in or accepted to an academic program pursuing an undergraduate or graduate degree.
- Must be returning to school the semester following the position or graduating after the position.
- Relevant majors include Pharmacy (PharmD), Biology, Chemistry, Biomedical Engineering, Statistics/Data Science, and Computer Science/Information Technology.
Nice To Haves
- Demonstrated leadership in campus activities, clubs, sports, current or previous work, or the community.
- Cumulative GPA of 3.0 or higher.
- Strong organization, Excel skills, and written communication.
- Interest in clinical research or drug development.
- Graduate student status may be better suited to one project.
Responsibilities
- Support clinical trial study start-up activities.
- Coordinate with contract research organizations (CROs) and vendors.
- Maintain trackers and metrics.
- Manage study documents.
- Capture lessons learned across drug programs.
- Assess study feasibility and potential trial sites.
- Communicate and coordinate with study teams while attending to compliance details.
Benefits
- Competitive and comprehensive total rewards package, which may include annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (medical, dental, vision, life, and disability), paid time off, and family support benefits.
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Education Level
No Education Listed
