Day-to-Day Responsibilities
Visit trial sites before, during and after a study to set up the trial, train site staff and monitor progress (site initiation and monitoring visits)
Review source documents such as patient records and compare them with the case report forms to verify data accuracy
Check that the trial follows the approved protocol, GCP guidelines and regulatory requirements
Track patient enrolment, visit schedules and timelines for each site you are assigned
Raise and follow up on queries, protocol deviations and safety reports with site staff and data management teams
Confirm that investigational product, consent forms and essential trial documents are in order and filed correctly
Prepare visit reports and update the sponsor or CRO on progress, risks and corrective actions


