Teams at ICON plc

Lead feasibility informatics strategy for clinical trial proposals and awarded feasibility projects. Provide data-driven feasibility analyses using internal/external data, support bid defenses, manage delivery and handover to site identification, assess risks, and collaborate with cross-functional teams to meet sponsor objectives.

Supports global clinical trials by coordinating study meetings, documents, reports, site activation, enrollment, monitoring, TMF reconciliation, vendor oversight, and study closeout activities. Maintains trial systems, investigator and site information, regulatory materials, clinical trial registry updates, and study communications. Contributes to document reviews, training materials, process improvements, and SOP revisions.

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%).