Clinical Trial Assistant

As a Clinical Trial Assistant at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

You will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Key Responsibilities:

• Coordinate study documents, trackers, meetings, and operational requests.
• Maintain accurate study information in relevant systems and repositories.
• Support site and study team communications and follow-up.
• Track actions, milestones, and outstanding documentation.
• Apply study procedures and escalate issues promptly.

Required Qualifications and Experience:

• 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.
• Clinical research, life sciences, healthcare, or relevant coordination experience.
• Knowledge of clinical trial documentation and systems.
• Experience coordinating study documents, trackers, meetings, and operational requests.
• Experience maintaining accurate study information in relevant systems and repositories.

Preferred Qualifications and Experience:

• ICH Good Clinical Practice (GCP) training.
• Clinical trial management systems (CTMS), electronic Trial Master File (eTMF), or electronic data capture (EDC) experience.
• Prior clinical trial assistant or study coordination experience.

Working Conditions:

• Willingness to travel as required (approximately 10%).

Rewards and Benefits:

• 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.