Clinical Trials Coordinator

3 weeks ago


Reading, Reading, United Kingdom ENGINEERINGUK Full time

Clinical Research Administrator

Company Overview

ICON plc is a world-leading healthcare intelligence and clinical research organization.

Job Summary

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc.

Key Responsibilities:
  • Coordinate all activities for setting up and monitoring a study, complete accurate study status reports and maintain study documentation.
  • Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.
Requirements:
  1. University degree in medicine, science, or equivalent.
  2. Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
  3. Excellent written and verbal communication in English.
  4. Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license.
What We Offer:
  • Competitive salary: £45,000 - £55,000 per annum.
  • Annual leave entitlements.
  • A range of health insurance offerings to suit you and your family's needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
  • Life assurance.
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.


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