Medpace Clinical Operations leverages our unique partnering philosophy and team structure to deliver effective, end-to-end collaboration, training, and resource planning around the globe. Working closely with the industry's top therapeutic and regulatory experts, our proficient and experienced team members engage quickly and provide strategic thinking – ensuring quicker start-up times, superior quality, and the most efficient delivery at every phase of trial.
Comprehensive communication throughout all phases of the clinical trial is essential to building successful partnerships – with Sponsors, research sites, and patients. Our dedicated teams are designed to serve as an extension of your team and provide unrivaled support at every stage of the drug development process. Medpace Clinical Research Associates (CRAs) work on fewer projects so they can really delve into your study and analyze the entire plan; and they work in concert with management across the globe ensuring you always receive the personalized service you deserve. Because we have one of the lowest turnover rates in the industry, you can enjoy continuity and peace of mind from development plan to product approval.
We share common goals and expectations regarding drug development and are committed to your success. Medpace Clinical Operations provides support in a number of critical areas, including:
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