Summer Intern, Clinical Trial Operations and Study Start-up

Regeneron

. Support operational work that gets clinical trials up and running and keeps them on track .

Posted 10/28/2026full-timeUnited StatesEntry Level💰 $18 - $51 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates strong organizational skills and proficiency in Excel for managing study documents and metrics in clinical trials. Effective communication and coordination with study teams and external vendors are essential for supporting operational activities and maintaining compliance.

Highest-signal resume keywords

Excel SkillsClinical Research InterestDocument ManagementStudy CoordinationLeadership Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Study Start-Up ActivitiesMetrics TrackingFeasibility AssessmentData ManagementClinical Trial Support

Soft Skills

Strong OrganizationWritten Communication

Industry Keywords

Contract Research OrganizationsDrug DevelopmentPharmacyBiologyChemistryBiomedical EngineeringStatisticsData ScienceComputer ScienceCompliance

About the role

Key responsibilities & impact

Support operational work that gets clinical trials up and running and keeps them on track
Support 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
Coordinate with study teams
Perform Excel and document management work
Communicate with study teams
Maintain compliance details

Requirements

What you’ll need

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: Pharmacy (PharmD), Biology, Chemistry, Biomedical Engineering, Statistics/Data Science, Computer Science/Information Technology
Demonstrated leadership in campus activities, clubs, sports, current or previous work, or the community preferred
Cumulative GPA of 3.0 or higher preferred
Strong organization, Excel skills, and written communication
Interest in clinical research or drug development is a plus
One project is better suited to a graduate student

Benefits

Comp & perks

Annual bonuses or other incentive plans
Equity awards
Pension or retirement benefits
401(k) company match
Health and wellness programs
Fitness centers
Medical, dental, vision, life and disability insurance benefits
Paid time off
Family support benefits
Inclusive culture
Reasonable accommodation for applicants with known disabilities or chronic illnesses