Clinical Trial 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.

What you will be doing

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.

• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.

• Support the preparation of study-related materials, such as informed consent forms and case report forms.

• Work with cross-functional teams to facilitate communication and ensure smooth trial execution.

• Contribute to the tracking and reporting of clinical trial metrics and milestones.