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 CRA at ICON, you will play a key role in ensuring data integrity, patient safety, and overall quality of oncology clinical trials conducted at investigative sites, 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 include:

• Conducting site qualification, initiation, monitoring, and close-out visits for oncology clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.