Site Management

At Croissance Clinical Research Africa, we specialize in providing comprehensive site management services, serving as the vital link between the study site, the sponsor, and the smooth conduct of clinical trials. Our dedicated team ensures seamless communication with every study site, from initial regulatory document collection to enrollment, follow-up, and project completion.

Recognizing the paramount importance of site training in ensuring proper study conduct and high-quality data collection, Croissance Clinical Research Africa prioritizes robust training programs for all site staff. Led by our experienced Project Managers and Clinical Research Associates (CRAs), these training initiatives ensure compliance with FDA, local regulatory, and ICH-GCP guidelines, as well as adherence to the study protocol and timely patient recruitment. We develop effective study protocol tools, newsletters, and subject enrollment aids to reinforce site staff training and enhance study performance.

Our proven site support model involves the placement of full-time, highly qualified clinical research coordinators at each study site. These dedicated professionals assist investigators and site staff with all day-to-day study conduct activities, ensuring smooth operations and adherence to protocol requirements. Additionally, we conduct weekly teleconferences with each site throughout the project duration, providing an opportunity to review study progress, address CRF and query completion, and assist with protocol queries and other study-related activities, thereby ensuring timely progress.

Croissance Clinical Research Africa guarantees that all study information is current, prioritized, and readily available to sponsors for effective site management. With our expertise and commitment to excellence, we ensure that your clinical trials proceed smoothly, meeting timelines and delivering high-quality results. Partner with us for expert site management services tailored to meet your study needs.