Identify the protocol deviations and record them in Database or eDC (electronic data capture). eDCs are the tool to capture clinical trial-related data.
Visit reports are prepared by clinical research associates.
Answer the queries raised by site staff such as CRC (clinical research coordinator).
They ensure data collected is accurate and verifiable. it is also called source data verification.
Depends on designation, they can manage clinical trial site payments and handle any ongoing negotiations.
Important documents archival are done by CRA.
They update the site contact list.
They respond to data management, Safety and other department queries as well.