Clinical Trial Associate

Employment type: Permanent. Requisition: JR159555. 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.

As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include

• - 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.

Your Profile

You will bring relevant clinical research experience, along with the following qualifications and skills1 …