Teams at ICON plc

Lead sponsor-side clinical study oversight, managing CROs and vendors (e.g., biometrics, IXRS, eTMF, central labs). Ensure protocol adherence, timelines, budgets, monitoring report review, eTMF/TMF compliance, site readiness, invoice approvals, risk management, audits/inspections, registry updates, and mentor junior team members.

Lead and perform clinical trial monitoring for Phase I oncology studies, ensuring GCP and protocol compliance. Conduct site visits, manage multiple sites, provide training and guidance to site staff and junior CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships. Frequent travel (~60%) required.

Lead monitoring activities for Phase I oncology clinical trials, ensure GCP/regulatory compliance, conduct site visits, train and guide site staff and other CRAs, manage multiple sites, collaborate with cross-functional teams, and maintain data integrity while traveling to sites (~60%).