Clinical Site Monitoring

Every blueprint for successful clinical site monitoring begins with the comprehensive training and valuable medical experience of Clinical Research Associates (CRAs). The CRAs at Encorium have extensive medical experience and are familiar with regulatory and GCP requirements as well as source documents. Our CRAs are local residents of the countries in which our studies are conducted and they understand the importance of developing a rapport with site staff to ensure effective communication and integration of services.

At Encorium, we create a site monitoring plan for each clinical trial that requires seamless implementation by CRAs. Our CRAs are process driven, trained to be logical and methodical in their approach, and empowered to proactively address any clinical site issues that may occur.