Our sites demonstrate a distinctive blend of physician expertise and patient demographics, meeting the criteria of over 300 clinical trials annually.

Using standardized processes, regulatory and finance staff consistently meets and exceeds industry standards for completion of regulatory approval and contract execution. In 2010, the affiliated group averaged 22 days for regulatory submission-to-approval, and 27 days for contract and budget receipt-to-execution.

Study teams focus on enrollment, retention, clean data, and striving to provide a professional, “monitor-friendly” environment and enhanced investigator accessibility. As a result of proven success in previous trials, the greatest number of awarded studies (2010) continues to be principal investigator invitations from sponsors (76%). Clinical research associates also provide a large number of trials through contact with study coordinators (12%).

To ensure all affiliated investigators are trained according to Good Clinical Practices, Encore Research, a division of JCCR, promotes a unique interactive investigator symposium featuring key industry leaders. Sponsor and CRO grants and support are greatly appreciated. Click here to learn more about Clinical Research Training for Physicians and additional educational opportunities.