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 a hybrid setting, collaborating with cross‑functional teams to ensure trials are conducted according to protocol and regulatory standards.

Key responsibilities

• Assist in coordinating and administering clinical trials, maintaining compliance with protocols and regulations.
• Organize and manage trial documentation, including study files, essential documents, and regulatory submissions.
• Prepare study materials such as informed consent forms and case report forms.
• Facilitate communication between stakeholders to ensure smooth trial execution.
• Track and report 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.
• Ability to work collaboratively in a fast‑paced environment with attention to detail.
• Willingness to travel up to 10% as needed.

Required skills

What we offer

• Competitive salary and a comprehensive benefits package.
• Annual leave entitlements and health insurance options for you and your family.
• Retirement planning, employee assistance programme, and flexible, country‑specific perks such as childcare vouchers, gym discounts, and travel subsidies.
• An inclusive culture that values diversity, high performance, and professional growth.