Jobs at ICON plc

The Clinical Trial Contract Associate manages site contract activities, drafting and negotiating agreements, collaborating with teams, and ensuring compliance with regulations.

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

As a Senior Clinical Research Associate, you'll oversee clinical trial activities, ensuring compliance with protocol and regulatory standards while managing site performance and supporting trial execution.

As a CRA II, you will design and analyze clinical trials, conduct site visits, ensure protocol compliance, and collaborate with investigators while maintaining data integrity and patient safety.