Clinical Trial Coordinator

3 weeks ago


Maidenhead, Windsor and Maidenhead, United Kingdom Fortrea Full time
Clinical Trial Administrator Job Description

Fortrea is seeking a skilled Clinical Trial Administrator to join our team in London. As a leading global contract research organization, we provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across multiple therapeutic areas.

Key Responsibilities:
  • Act as the primary contact for project teams and study sites, ensuring seamless communication and coordination.
  • Perform complex data review and management tasks, adhering to established guidelines and regulations.
  • Assist with the management of study supplies, including organization and shipment coordination.
  • Develop, update, and maintain study-specific trial management files, tools, and systems.
  • Support local project team members with administrative tasks, such as payments to investigators, client correspondence, and status report preparation.
  • Coordinate meetings with clients, investigators, and project teams, including minute-taking and follow-up actions.
  • Ensure compliance with Fortrea SOPs, FDA, ICH, and GCP regulations in all aspects of daily work.
  • Contribute to the development of Monitoring Conventions as assigned.
  • Assist with submissions and notifications to Ethics Committees and Regulatory Authorities.
Requirements:
  • A minimum of 12 months of Clinical Research Admin experience from a CRO or Pharma company.
  • Basic understanding of biology and biological processes.
  • Excellent organizational and time management skills.
About Fortrea:

Fortrea is a global contract research organization dedicated to revolutionizing the development process. We strive to deliver life-changing ideas and therapies to patients in need. As an Equal Opportunity Employer, we value diversity and inclusion in the workforce and do not tolerate harassment or discrimination of any kind.



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