Clinical Trials Coordinator

1 day ago


Reading, Reading, United Kingdom ENGINEERINGUK Full time

Clinical Research Administrator Role at ICON plc

Engineer clinical trials to shape the future of healthcare with us.

About Us

We are a leading provider of healthcare intelligence and clinical research services. Our mission is to foster an inclusive environment driving innovation and excellence, while delivering exceptional results for our clients.

The Opportunity

We are seeking a skilled Clinical Research Administrator to join our dynamic team in Reading, UK. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

Key Responsibilities:
  1. Coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.
  2. Ensure patient safety by enforcing ICON's procedures, protocols, and regulatory requirements.
Your Profile:
  1. University degree in medicine, science, or equivalent.
  2. Knowledge of ICH-GCP guidelines and expertise to review and evaluate medical data.
  3. Excellent written and verbal communication skills in English.
  4. Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license.
Compensation and Benefits:
  • A competitive salary: £55,000 - £65,000 per annum, depending on experience.
  • Varying annual leave entitlements.
  • An extensive range of health insurance offerings.
  • Competitive retirement planning options.
  • A Global Employee Assistance Programme (EAP).
  • Lifelong learning opportunities.


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