Teams at ICON plc

Conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance, data integrity, and patient safety. Review and resolve data queries, collaborate with investigators and site staff, and contribute to study documentation including protocols and clinical study reports. Role requires frequent travel and independent monitoring experience.

Lead cross-functional study teams to plan, execute, and close regional/global clinical trials. Manage scope, timelines, risk mitigation, budgets, enrollment strategy, vendor/TPO oversight, Trial Master File readiness, training coordination, and stakeholder communication to deliver quality trials on time and within budget.

Senior Site Monitor responsible for planning and conducting on-site and remote monitoring across Phase I-IV studies. Ensures site compliance with protocol, data quality, and participant safety, conducts source data verification, manages site communications, supports RBQM processes, and participates in audits and inspections.