Clinical Trial Associate

About the role

ICON is seeking a Clinical Trial Associate to support the design and analysis of clinical trials, interpret medical data, and help advance innovative treatments.

Key responsibilities

• 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.

Required profile

• Bachelor's degree in a scientific or healthcare‑related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast‑paced environment with attention to detail.

What we offer

• Competitive salary and a range of health insurance options for you and your family.
• Various annual leave entitlements and flexible, country‑specific benefits such as childcare vouchers, gym memberships, and travel passes.
• Global Employee Assistance Programme providing 24‑hour support for well‑being.
• Retirement planning offerings and life assurance.