Cincinnati, Ohio, US (On-site)6 open jobs
Medpace is a full-service CRO running clinical trials, central and bioanalytical labs, imaging and cardiac safety core labs, Phase I research, and a CTMS for biotech, pharma, and medical device clients worldwide.
Medpace, Inc. runs the infrastructure behind other people's clinical trials. Founded in 1992 in Cincinnati by August J. Troendle, it is a full-service contract research organization that takes therapeutics through clinical development for biotechnology, pharmaceutical, and medical device clients. The data picture is the interesting part: a central laboratory handling trial sample analysis, a bioanalytical laboratory, an imaging core laboratory reviewing trial imaging, a cardiac safety core laboratory, a dedicated Phase I unit for early-phase studies, and a clinical trial management system (CTMS) that ties trial execution together. That is patient data, sample data, imaging data, and cardiac safety data moving through connected systems across every phase of development.
The operational footprint is distributed. Medpace describes personnel, offices, and investigator relationships across four major regions - North America, Europe, Latin America, and Asia Pacific - with the headquarters and founding location in Cincinnati. Regulatory affairs, clinical operations, and patient recruitment (with a stated focus on diversity in recruitment) sit alongside the laboratory and core lab services, so the workflow spans therapeutic, regulatory, and operational expertise rather than a single system. Growth has been entirely organic: more than three decades in operation with no mergers and acquisitions, which means fewer inherited environments and more continuity in the systems and teams that exist.
Medpace positions itself as an extension of its clients' teams, combining local expertise with global resources under a scientifically driven, full-service model. The stated mission is accelerating the global development of safe and effective medical therapeutics. For anyone working on the security side of that, the concrete domains are clinical trial management, central and bioanalytical laboratory services, imaging and cardiac safety core labs, Phase I research, and the regulatory and clinical operations workflows that surround them.
