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4worldlovers: Driven by a full-service CRO model that coordinates and integrates all services for our clients, Medpace provides an accountable, seamless, integrated, and efficient platform for executing clinical research – increasing quality and speed while significantly reducing the need for duplicate management oversight. More than a “set of extra hands”, we are an extension of your team – embedding medical, regulatory, and operational expertise into your trials to navigate and overcome challenges. It’s how we make the complex seamless. And it’s why we are

Medpace employs a high-science and disciplined operating approach that leverages regulatory and therapeutic expertise across all major therapeutic areas. For sponsors, this means your clinical trial will be led by a collaborative team of medical, operational, and regulatory experts with deep knowledge and insights about the disease and the patients your clinical trial is targeting. Backed by over 30 years of experience, our relationships with Key Opinion Leaders, Principal Investigators, and high-performing sites help accelerate clinical development.

When you partner with Medpace, you get guidance from our cross-functional team of experts who work together—combining our experience and perspectives—to guide and accelerate your compound through clinical development. This “cross-pollination” of experts from numerous functional areas—including medical, regulatory, operations, labs, and imaging—allows us to apply our experience and relationships to an extensive range of diseases. As a full-service CRO with labs, imaging, a phase I unit, and cardiac safety capabilities, we offer comprehensive services and the support of our collective expertise to accelerate your studies and programs.

Because almost every clinical trial requires laboratory support, having wholly-owned entities with a broad range of capabilities and comprehensive test menus provides built-in efficiencies and collaboration. In concert with the Medpace CRO or working on standalone projects, experts from our central laboratories and bioanalytical laboratory can help plan and execute your testing needs.


A collaborative approach – Sponsors, Medpace, and Sites working together to achieve diversity, equity, and inclusion in clinical trials.


A customized approach – incorporating DCT capabilities to tailor a best-fit trial design to your program’s objectives and position your trial for success.

Enabling the continuous collection and real-time transmission of patient biomarker data to provide vital operational and analytical advantages.