Clinexa has unique site management capabilities. Our Site Management (SMO) work force is clinically knowledgeable, meaning that their methods are not only innovative but also in tune with the needs of clients, patients, and investigators and strictly compliant with the Indian and ICH-GCP.
We appoint a full-time, highly qualified clinical research coordinator at each study site to assist and support the investigators and site staff with all study related activities, ensuring compliance with FDA, local regulatory and ICH-GCP guidelines and an efficient completion of assigned duties. Our site coordinators have a strong personal ethics, clinical competency, people skills, patience and flexibility. Our CRCs are dedicated, detail oriented and have an operational knowledge of the research process and institutional infrastructure.
Our up-gradation of the research sites is a continuous process according to the study specific requirements so that the studies conducted are streamlined with efficient site services that expedite recruitment and study execution.