Teams at ICON plc

Lead and conduct clinical trial monitoring for oncology studies, ensuring GCP and protocol compliance. Manage multiple sites, perform site visits, resolve issues, support data integrity and reporting, train site staff and mentor other CRAs, and collaborate with cross-functional teams to maintain trial quality.

Lead onsite and remote monitoring for oncology clinical trials, ensuring data integrity, subject safety, TMF reconciliation, regulatory readiness, site activation, training, KRI monitoring, CAPA implementation, and site relationship management.

Lead site-facing clinical monitoring for oncology studies: conduct selection, initiation, routine monitoring, and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor safety and drug accountability; support recruitment/retention; resolve data queries; escalate risks and coordinate with cross-functional clinical teams.