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 2 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.
Our 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.