We are seeking a Clinical Trial Associate to join our diverse and dynamic team. As a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.
Requirements
- 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.
Benefits
- Annual leave entitlements
- Health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits