Regulatory Research Intern- Summer 2026

Medpace, Inc.•Cincinnati, OH

23d•Onsite

About The Position

Our clinical operations activities are growing rapidly, and we are seeking a full-time, office-based intern to support our Regulatory Submissions team within our Site Activation and Maintenance (SAM) Department for summer 2026. This group plays a key role in the study start-up/site activation process at Medpace by communicating with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in a clinical trial. The Regulatory Submissions Intern will provide support to the Regulatory Submissions Coordinators and Managers as they maintain start-up timelines, review and collect regulatory documents, and proactively identify solutions to regulatory issues.

Requirements

High School Diploma, pursuing Bachelors degree in life science field
Graduating in December 2026 or May 2027
Excellent organizational and prioritization skills
Knowledge of Microsoft Office
Availability to work full-time (40 hours/week) in our Cincinnati, OH office.

Responsibilities

Provide support to the study start-up team through completion of compliance tasks
Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF)
Gain hands-on training and exposure to the clinical trial start-up phase through our Site Activation & Maintenance (SAM) Training Program as outlined below.