Medical Trial Coordinator

2 months ago


Reading, Reading, United Kingdom ICON plc Full time

ICON plc is a world-leading healthcare intelligence and clinical research organization, headquartered in the UK.

We are currently seeking a Clinical Research Associate to join our dynamic team. This role involves overseeing and coordinating clinical trials, ensuring compliance with regulations and collecting critical data.

Job Summary:

This is a full-time position that requires excellent organizational and communication skills, as well as the ability to work independently and as part of a team.

Responsibilities:
  • Coordinate all aspects of clinical trial setup and monitoring, including study documentation and status reporting.
  • Ensure compliance with ICON's procedures, protocols, and regulatory requirements.
Requirements:
  • A bachelor's degree in medicine, science, or a related field.
  • Knowledge of ICH-GCP guidelines and experience in reviewing and evaluating medical data.
  • Fluent written and verbal communication skills in English.
  • Valid driver's license and willingness to travel internationally (at least 60% of the time).

Salary: £45,000 - £55,000 per annum, depending on experience.

Benefits: Comprehensive benefits package, including annual leave entitlements, health insurance, retirement planning, and employee assistance programs.



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