Clinical Trial Associate

• 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
• Work in a sponsor-dedicated model supported by ICON’s global expertise
• Work for a global, science-led, patient-focused pharmaceutical company with offices in the region of Brussels