Principal Clinical Research Associate

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 Principal CRA at ICON, you will oversee and manage clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards.

**What You Will Do:**

Your focus will be on coordinating clinical trial monitoring delivery, resolving issues, and developing team capability.

Key responsibilities include:

+ Leading site management activities, including site selection, initiation, monitoring, and close-out visits, to ensure compliance with study protocols and regulatory guidelines.
+ Serving as the primary point of contact for clinical sites, addressing site queries, and reso...