Medpace

Add a review
  • 1,000 - 50,000 employees

Regulatory Research Intern - Summer (Jun 2026)

Location details

On-site

  • United States

    United States

    • Ohio

      Cincinnati

Location

Cincinnati

Closing in 2 months

Opportunity details

  • Opportunity typeInternship, Clerkship or Placement
  • Application open dateApply by 15 Apr 2026
  • Start dateStart date 1 Jun 2026 - 30 Jun 2026

Support the Regulatory Submissions team in clinical trial start-up activities at Medpace’s Cincinnati office for summer 2026.

Your Role

Here’s what you will be doing:

  • Provide support to the study start-up team through the completion of compliance tasks
  • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF)
  • Support Regulatory Submissions Coordinators and Managers in maintaining start-up timelines and reviewing regulatory documents
  • Proactively identify solutions to regulatory issues
  • Communicate with research sites to collect essential documents before site activation

About You

The company is looking for:

  • High School Diploma and currently pursuing a Bachelor’s degree in a 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 the Cincinnati, OH office

Compensation & Benefits

  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms, and attractions
  • Modern, eco-friendly campus with an on-site fitness center
  • Discounted tuition for University of Cincinnati online programs

Training & Development

Gain hands-on training and exposure to clinical trial start-up through the Site Activation & Maintenance (SAM) Training Program, which includes:

  • Independent learning modules, interactive exercises, and team workshops
  • Exposure to real-world tasks via a robust mentoring program
  • Core curriculum designed to advance professional learning and employee performance

Career Progression

  • Structured career paths with opportunities for professional growth within Medpace’s clinical operations and regulatory teams.

How to Apply

  • Submit your application according to the company's guidelines, ensuring that all required information is included.
  • A Medpace team member will review your qualifications and contact you with details for next steps if interested.

This job may close before the stated closing date, you are encouraged to apply as soon as possible.

Report this job

Work rights

The opportunity is available to applicants in any of the following categories.

Work right - United States
United States
US CitizenUS Permanent ResidentUS Student Visa

Qualifications & other requirements

You should have or be completing the following to apply for this opportunity.

Degree or Certificate
Qualification level
Qualification level
Bachelor or higher
Study field
Study field (any)
Sciences
  • Biology
  • Chemistry
  • Physics
  • Sciences (all other)

Hiring criteria

  • Experience requirementNo experience required
  • Working rights
    US Citizen
  • Study fields
    Sciences
  • Degree typesBachelor or higher
Show all hiring criteria

Reviews

user
user
user
Show all reviews

About the employer

logo-medpace-450x450-2024

Medpace USA

Number of employees

1,000 - 50,000 employees

Industries

Pharmaceuticals

Medpace USA offers diverse career opportunities in clinical research and development, supporting pharmaceutical and biotechnology advancements globally.