Clinical Trial Management & Logistics

  • Protocol writing
  • Costings for grant applications
  • HRA/ethics/IRAS submissions
  • Sponsor oversight
  • Risk assessments
  • Close collaboration with chief investigator, data manager, study statistician and trial co-ordination staff
  • Trial Management Group and Investigator meeting support
  • Multicentre site setup, monitoring and close out
  • Pharmacovigilance
  • Archiving
  • Working in accordance with CTU SOPs

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