Clinical Research Coordinator

2 months ago

Reading, Reading, United Kingdom ICON Plc Full time

Job Summary:

ICON Plc is seeking a highly skilled Clinical Research Associate to join our dynamic team. 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:

  • Coordinate all activities for setting up and monitoring a study, completing accurate study status reports, and maintaining study documentation.
  • Run sponsor-generated queries efficiently and take responsibility for study cost efficiency.
  • Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Requirements:

  • University degree in medicine, science, or equivalent.
  • Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
  • Excellent written and verbal communication in English.
  • Good social skills enabling you to deal with queries in a timely manner.
  • Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license.

What We Offer:

  • Competitive salary.
  • Various 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.

Equal Opportunities Employer:

ICON Plc is an equal opportunities employer and welcomes applications from all qualified candidates without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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