Teams at ICON plc

Lead clinical trial monitoring activities to ensure protocol and regulatory compliance, conduct site visits, resolve issues, support data integrity, train site staff and CRAs, collaborate cross-functionally, and maintain strong site relationships to drive successful trial execution.

Conduct site qualification, initiation, monitoring, and close-out visits for oncology clinical trials. Ensure protocol compliance, data integrity, and patient safety; perform data review and query resolution; collaborate with investigators and site staff; and contribute to study documentation and clinical study reports.

The Clinical Research Associate will oversee site compliance, conduct visits, monitor patient safety, and collaborate with cross-functional teams in clinical studies.