Overview

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.

About the Role

As a CRA II at ICON, you will design and analyse clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key Responsibilities

• Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
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