Teams at ICON plc

Serve as primary contact between investigational sites and sponsor to conduct site selection, initiation, routine monitoring, and close-out. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety (AE/SAE/PQC), support recruitment and drug accountability, resolve data queries, track site training and budgets, escalate risks, and collaborate with cross-functional clinical teams.

Lead on-site monitoring for oncology clinical trials: site selection, initiation, routine monitoring, and close-out. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety and drug accountability, support recruitment/retention, resolve data queries, escalate risks, and coordinate site budgets and cross-functional teams.

Lead on-site clinical monitoring for oncology/hematology trials: conduct site selection, initiation, routine and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor patient safety and AE/SAE reporting; oversee drug accountability, support recruitment and retention, resolve data queries, track site budgets, and escalate risks to clinical teams while collaborating cross-functionally.