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 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.

Lead and perform clinical trial monitoring to ensure protocol, regulatory, and GCP compliance. Conduct site visits, assess performance, resolve issues, support data integrity, collaborate with cross-functional teams, train and mentor site staff and other CRAs, and maintain stakeholder relationships to drive successful trial execution. Focused on oncology and other therapeutic areas on the West Coast.