Jobs at ICON plc

As a Clinical Research Associate, you'll conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with investigators.

Oversee clinical trial monitoring activities across study sites, ensuring protocol adherence, regulatory compliance, data integrity, and Good Clinical Practice standards. Conduct site visits, resolve performance issues, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships. The role requires independent management of multiple sites and projects, strong organizational and communication skills, and approximately 60% travel.

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.