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Medpace International Employee Reviews, Feedback, Testimonials

Clinical research (CRO)Cincinnati, USA1,001-5,000 employees
3.8
4 reviews

About Medpace International

Medpace International is the global arm of Medpace, a full-service clinical research organization that manages multinational clinical trials for biotech, pharmaceutical and medical device sponsors. Operating across Europe, Asia-Pacific and the Americ...

Detailed Employee Ratings

3.5
Work-Life Balance
3
Compensation
3.8
Company Culture
4
Career Growth
3.8
Job Security

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4 reviews found

Employee Reviews (4)

Read authentic experiences from current and former employees at Medpace International

3.0
Verified Anonymous

Site Coordinator Review

Clinical OperationsFull-timeHybrid
Aug 20, 2025

What I liked

Good hands-on experience with sites and patient interaction. Colleagues were helpful and training was adequate for the role.

Areas for improvement

Long hours during peak study phases, limited salary progression and promotions felt hard to come by. Internal communication can be inconsistent between teams.

3.0
Verified Anonymous

Project Manager Review

Project ManagementFull-timeHybrid
Jul 2, 2025

What I liked

Good exposure to global projects and a variety of therapeutic areas. Hybrid work allowed decent flexibility and colleagues were collaborative.

Areas for improvement

Decision-making can be slow and processes are sometimes bureaucratic. Limited merit increases during my time there.

4.0
Verified Anonymous

Senior Clinical Research Associate Review

Clinical OperationsFull-timeOn-site
Mar 15, 2025

What I liked

Strong clinical exposure, very supportive site teams and clear SOPs. Lots of on-the-job learning and opportunities to travel to different sites.

Areas for improvement

Heavy travel schedule can be tiring and salary growth is slower than industry peers.

5.0
Verified Anonymous

Regulatory Affairs Specialist Review

Regulatory AffairsFull-timeRemote
Jan 20, 2025

What I liked

Flexible remote setup, excellent mentorship and training programs. Strong focus on compliance and career growth — I've taken on meaningful regulatory submissions quickly.

Areas for improvement

Occasional late timezone meetings and busy periods around submissions, but manageable overall.

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