About
The Certification in Clinical Trial Monitoring & Coordination is a 6-hour self-paced course designed to help you master the core responsibilities of Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), and Site Coordinators. You’ll learn how to: • Understand trial protocols, ICFs, and regulatory documents • Monitor site activities, ensure data accuracy, and verify source documents • Coordinate patient visits, site readiness, and study tracking • Handle adverse events, deviations, and implement CAPA processes • Prepare sites for audits, inspections, and trial close-out Who is this for? Life science, pharmacy, nursing, MBBS graduates, or anyone aiming to start a career as a CRA, CRC, or Trial Assistant. What’s included? • Monitoring visit checklists & deviation log templates • Mock monitoring reports and practice workflows • Visual workflows for trial coordination & documentation