Teams at ICON plc

Support coordination and administration of clinical trials, maintain trial documentation, prepare study materials, assist regulatory submissions, liaise with cross-functional teams, and track trial metrics and milestones.

Serve as primary ICON liaison to investigator sites, build/maintain site relationships, support multiple studies, coordinate with clinical teams, monitor site performance and start-up timelines, gather site feedback, and drive site engagement and improvement actions.

Support site activation, documentation, and site communications for clinical trials. Maintain site records and trial systems, coordinate site visits and logistics, assist CRAs and project teams, support site payments, ensure audit-ready filing, and contribute to process improvements to enhance site support efficiency.