Jobs at ICON plc

As a Clinical Research Associate 2, you will monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring compliance with protocols and regulations, mentoring staff, and maintaining site relationships while overseeing multiple projects.

As a Clinical Research Associate, you will coordinate clinical trials, ensure regulatory compliance, and maintain study documentation, while establishing relationships with stakeholders.

As a Sr CRA, you will monitor clinical trials, ensure compliance with protocols and regulations, support site staff, and manage relationships with sites and stakeholders.