Teams at ICON plc

Conduct and manage site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; review and resolve data queries; collaborate with investigators and prepare study documentation and reports. Role requires extensive travel and independent monitoring experience.

Serve as primary site contact and perform site selection, initiation, routine monitoring, and close-out visits. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety and reporting, support recruitment and drug accountability, resolve data queries, track site budgets/payments, and escalate risks while collaborating with cross-functional clinical teams.

The Senior CRA will oversee clinical trial activities, ensuring adherence to protocols and regulatory requirements while managing multiple sites and projects.