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Information for collaborators

ICR-CTSU works with individual clinicians located across the UK and in close conjunction with the relevant NCRI Clinical Studies Groups to help formulate and drive national clinical research portfolios.

We also collaborate with national and international collaborative groups and trials units to conduct trials within the international framework.

Our team of experienced statisticians, trial managers, data managers, clinical IT systems and administrative staff supports the full trial life cycle from initial discussions of trial concept, through design and development, day-to-day management, to analysis and reporting.

Areas of expertise

ICR-CTSU staff have expertise in the design, central management and analysis of clinical trials, including the following:

  • Statistical design and sample size calculation
  • Protocol development
  • Preparation of funding applications
  • Design of case report forms
  • Development of specialist clinical trials IT systems
  • Central trial management and monitoring
  • Data and sample collection
  • Data management and monitoring
  • Quality assurance and regulatory affairs
  • Analysis and reporting

We are always interested in discussing new studies that would fit within our portfolio. For more information please take a look at the following documents and then get in touch with the ICR-CTSU team

Current vacancies

Clinical trials

Division of Clinical Studies

The division carries out or coordinates high-quality trials and translational research at both an early phase – typically to test new targeted drugs – and a later stage.