Clinical Trial Associate

About the role

ICON plc is seeking a Clinical Trial Associate to support the design, execution, and analysis of clinical studies. You will work in an office‑based environment, collaborating with cross‑functional teams to ensure trials run smoothly and comply with all regulatory requirements.

Key responsibilities

• Assist in coordinating and administering clinical trials, ensuring protocol and regulatory compliance.
• Maintain and organize trial documentation, including study files, essential documents, and regulatory submissions.
• Support preparation of study materials such as informed consent forms and case report forms.
• Facilitate communication between functional teams to promote efficient trial execution.
• Track and report 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 abilities.
• Detail‑oriented and able to work collaboratively in a fast‑paced environment.

Required skills

What we offer

• Competitive salary and a comprehensive benefits package.
• Annual leave entitlements and flexible health‑insurance options for you and your family.
• Retirement planning programs and life assurance.
• Global Employee Assistance Programme and a range of optional benefits such as childcare vouchers, bike purchase schemes, gym discounts, and travel subsidies.