Our proven comprehensive site support model involves placing a full-time, highly qualified clinical research coordinator at each study site to assist the investigators and site staff with all day-to-day study conduct activities. In addition, weekly teleconferences are scheduled with the site throughout the project that allows our staff to review study status, CRF and query completion and assist with protocol questions and any other study related activities to ensure the study proceeds in a timely manner. Croissance Clinical Research ensures all study information is current, prioritized, and available to Sponsors for effective site management.
Croissance Clinical Research performs site management services to act as the liaison between the site, the sponsor and the conduct of the study. We do this by continuous communication with every study site, starting with the collection of regulatory documents and continuing throughout enrollment, follow-up and project completion.
Croissance Clinical Research understands that site training is key to ensure proper study conduct, quality data collection and to keep our sponsors’ projects on top of the to-do list.
Our Project Managers and CRAs institute training programs for all site staff to ensuring compliance with FDA, local regulatory and ICH-GCP guidelines and adherence to the protocol as well as timely patient recruitment. We develop effective study protocol tools, newsletters and subject enrollment aids to reinforce site staff training.
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