Medpace Fall 2025 Regulatory Internships – Apply Now
Medpace, a globally recognized clinical research organization, is offering a Regulatory Research Internship for Fall 2025 at its Cincinnati, Ohio, campus. This internship is perfect for students pursuing a Bachelor’s degree in Life Sciences who are looking to gain real-world experience in clinical trials and regulatory documentation. Join a mission-driven team that advances drug development while enhancing your career with Medpace’s specialized Site Activation & Maintenance (SAM) Training Program.
About Medpace
Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With a mission to accelerate the global development of safe and effective medical therapeutics, Medpace leverages local regulatory and therapeutic expertise across major areas, including oncology, cardiology, and more. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people in 40+ countries.
Job Details:
Job Title: Regulatory Research Fall 2025 Intern
Location: Cincinnati, Ohio
Department: Site Activation & Maintenance
Job Number: 11168
Job Summary
Our clinical operations activities are growing rapidly, and we’re seeking full or part-time, office-based interns to support our Regulatory Submissions team within our Site Activation and Maintenance (SAM) Department during the summer 2025 semester. The Regulatory Submissions Intern will play a key role in maintaining start-up timelines, reviewing and collecting regulatory documents, and identifying solutions to regulatory issues.
Responsibilities
- Provide support to the study start-up team through the completion of compliance tasks
- Maintain and perform quality review of trial documents within the Trial Master File (TMF)
- Participate in the Site Activation & Maintenance (SAM) Training Program
Qualifications
- High School Diploma, pursuing a Bachelor’s degree in life science preferred
- Excellent organizational and prioritization skills
- Knowledge of Microsoft Office
- Availability to work a minimum of 20 hours per week in our Cincinnati, OH office. Full-time preferred.
SITE ACTIVATION & MAINTENANCE (SAM) TRAINING PROGRAM
- Complete learning modules, exercises, and workshops
- Participate in a mentoring program
- Gain exposure to real-world tasks in a clinical trial start-up
Cincinnati Perks
- Flexible work environment
- Competitive PTO packages
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Discounts on local attractions
Keywords: Medpace, Regulatory Research Intern, Cincinnati, SAM Department, Clinical Trials, Training Program
