ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Senior Clinical Research Associate at ICON, you will be responsible for the monitoring and oversight of clinical trial sites, ensuring studies are conducted in accordance with the protocol, ICH GCP, and applicable regulatory requirements. You will be embedded within ICON Strategic Solutions, working in partnership with a sponsor to deliver high-quality clinical research across the study lifecycle.

What You Will Do

In this role, you will take full ownership of investigator sites, leading monitoring activities and ensuring successful study delivery from start-up through to close-out.

Key Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visi...