Teams at ICON plc

Lead site management and monitoring for Oncology clinical trials, performing on-site and remote visits, ensuring data integrity and subject safety, managing TMF/essential documents, driving site activation and engagement, monitoring KRIs, implementing CAPAs, supporting IRB/EC submissions and regulatory inspections, and mentoring/joining oversight activities.

Oversee and monitor clinical trial sites to ensure GCP and protocol compliance, conduct site visits, resolve issues, ensure data integrity, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to support trial execution.

Lead and coordinate medical affairs projects and programmes, develop detailed plans, manage timelines/budgets/resources, lead cross-functional teams, monitor risks and progress, engage stakeholders, and prepare status reports while building team capability and resolving issues to ensure on-time, on-budget delivery.