Clinical Trial Administrator

1 day left

Up to £35,000 per annum
01 Feb 2021
03 Mar 2021
Jim Gleeson
Full Time
Contract Type
Experience Level
Experienced (non-manager)
CK Group are recruiting for a permanent Clinical Trial Administrator to join a novel and exciting biotech company based in Oxford, with an extensive range of products within their pipeline, both in pre-clinical and clinical development.

Clinical Trial Administrator Role:

As Clinical Trial Administrator you will support clinical activities across the company's R&D portfolio with regard to time, cost and quality and in accordance with SOPs, ICH-GCP guidelines and local regulations.

Key duties will include:
  • Tracking, distributing and filing documents.
  • Maintenance of the electronic Sponsor Oversight File and/or the Trial Master File.
  • Preparing and sending out study materials to Investigator Sites.
  • Tracking and processing Investigator Site payments, and raising purchase orders.
  • Assisting with the management of safety, including SUSAR reporting.
  • Supporting clinical staff within the department, archiving documentation, and facilitating coordination of ethical, country-specific regulatory and R&D submissions.

Your Background:
As Clinical Trial Administrator you will require the following:
  • At least 2 years of experience working in clinical research.
  • A good understanding of GCP and regulatory requirements.
  • Excellent time management and organisational abilities, and the ability to manage conflicting workloads.
  • A high level of computer literacy, including MS Office.
  • Ability to work in a small matrix team.
  • Preparing study materials to be sent Investigator sites.
  • A highly effective communicator, both verbal and written.

For more information or to apply for this Clinical Trial Administrator position, please contact CK Group, quoting job ref 49342.

It is essential that applicants hold entitlement to work in the UK.

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