Clinical Trial Assistant

About the role

Join ICON's sponsor‑dedicated model as a Clinical Trial Assistant, supporting the design and analysis of clinical trials and contributing to innovative treatments that benefit patients worldwide.

Key responsibilities

• Assist in coordinating and administering clinical trials, ensuring protocol and regulatory compliance.
• Maintain and organize trial documentation, including study files and regulatory submissions.
• Support preparation of study materials such as informed consent forms and case report forms.
• Facilitate communication with cross‑functional teams to ensure smooth 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 skills.
• Ability to work collaboratively in a fast‑paced environment with attention to detail.
• Willingness to travel up to 10% as required.

What we offer

• Competitive base salary and performance‑related incentives.
• Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.
• Retirement and pension plans, life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.