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.

As a CRA II, you'll conduct and monitor clinical trials, ensure compliance and data integrity, and collaborate with site staff and investigators.

Serve as primary ICON liaison to investigator sites, build strong long-term relationships, support multiple studies, align site capabilities with study needs, monitor site performance and metrics, drive improvements, and contribute to site engagement strategies and process enhancements.