Clinical Trial Coordinator

3 days ago

London, Greater London, United Kingdom ICON Full time
Clinical Trial Coordinator

ICON is seeking a highly motivated Clinical Trial Coordinator to join our team. The successful candidate will be responsible for managing all documents and logistical tasks related to trial feasibility, start-up, execution, and close-out of clinical trials.

Key Responsibilities:

  • Ensure trial-related activities are compliant with GCO SOPs, policies, code of Good Clinical Practice (GCP), Health Care Compliance requirements (HCC), and local regulatory requirements.
  • Manage all documents and logistical tasks related to trial feasibility, start-up, execution, and close-out of clinical trials.
  • Collaborate with the Clinical Trial Managers and CRA's to ensure overall site management while performing trial-related activities for assigned protocols.

Requirements:

  • Degree in the life sciences.
  • Minimum of 1-2 years of previous proven CTA experience in a CRO or Pharmaceutical environment.
  • Great planning and organizational skills.
  • Strong administrative skills.
  • Organizational skills to support several team members.
  • Excellent written and verbal communication in English and Hebrew.
  • Working knowledge of computer systems including Microsoft Word, Excel, Outlook, and PowerPoint.

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