QR code linking to this job posting Clinical Trial Coordinator in 317 02 Royal Victoria Infirmary in317 02 Royal Victoria Infirmary PUBLISHED FRI 17 JAN 2025

Band 5: £29,970 to £36,483 a year per annum  PERMANENT 

The NIHR Newcastle Clinical Research Facility (NCRF) delivers high-quality, cutting-edge experimental medical research and early phase clinical trials across a wide range of speciality areas. The NCRF is established by the partnership between Newcastle University and the Newcastle upon Tyne Hospitals NHS Foundation Trust, both founding members of the Newcastle Health Innovation Partners, one of only eight Academic Health Science Centres in the UK.

NCRF is looking for a Clinical Trial Coordinator to join the team, to support the set-up and delivery of the wide portfolio. This role will be based within the Royal Victoria Infirmary Research Unit (RVRU), Leazes Wing, Royal Victoria Infirmary.

  • Interview Date Thursday 13 February 2025
  • 37 Hours 30 Minutes/Week
  • You will be redirected to Trac to apply for the vacancy. Please expand the job details section and read all of the information before applying for the vacancy.

NO AGENCIES PLEASE

The successful candidate will be highly motivated with excellent communication and interpersonal skills. Working in a busy environment with a commitment to collaboration, along with knowledge of Good Clinical Practice, Research Governance Framework and Data Protection Act. You will be able to demonstrate advanced IT skills particularly Microsoft Office. This is a demanding role which requires an organised individual with the ability to work under pressure.

About us

  • To ensure any trials within the post holders remit, carried out in the Clinical Trials Unit are properly conducted according to Good Clinical Practice (GCP), Research Governance Framework and are compliant with the EU directive for clinical trials. (There can be multiple trials at any given time, in various stages of preparation,inception and completion.)
  • All events pertaining to the treatment of said patients are reported in the agreed timeframes to relevant external trials organisations.

As a flexible working friendly organisation, we want to be sure that you can work in a way that is best for us and for our patients, and for you. Speak to us about how we might be able to accommodate a flexible working arrangement. If it works for the service, we will do our best to make it work for you.