Clinical Monitoring

Every Medpace Clinical Research Associate (CRA) receives comprehensive, hands-on training in an individualized curriculum based on their healthcare background and industry experience. Through the Medpace Global Training and Development program, CRAs gain a deep understanding of each protocol, standard operating procedures (SOPs), and how to accelerate your drug towards approval. Ongoing study-specific training led by the industry’s top therapeutic and regulatory experts ensures each associate is an expert on your protocol.

Medpace CRAs are dedicated to an average of only two protocols at a time, empowering them to focus on process excellence, understanding the intricate issues of the protocol and/or indication (disease), and ensuring site compliance.
The Medpace unique team structure is designed to be the most streamlined in the industry. Reporting lines are clear, open and transparent for everyone involved – guaranteeing appropriate support and oversight for each CRA.