HRB CRCI National Study Feasibility Programme

Study feasibility is a process through which a clinical trial sponsor (or representative e.g. Clinical Research Organisations) identifies potential investigator sites and evaluates if they are suitable to conduct the clinical trial. HRB CRCI provides a service to streamline the clinical trial investigator site identification and study feasibility process nationally, delivering consistency and efficiency in the process.  Our study feasibility service is free of charge with an aim of secure more research opportunities for Irish patients and to ensure that Ireland is recognised internationally as a preferred location for clinical trials and covers all disease areas.

The HRB CRCI National Study Feasibility Programme connects academic and industry sponsors with potential investigators. HRB CRCI act as the channel through which study feasibility assessments can be distributed and completed efficiently. The HRB CRCI Investigator Membership Database and Clinical Research Facility/Centre (CRF/C) network is utilised to significantly reduce the time taken to identify investigator sites and to assess study feasibility. For Oncology Studies, we collaborate with Cancer Trials Ireland and Cancer Trials Research Units across Ireland on these feasibility assessments.

The programme is actively managed by the Clinical Trial Liaison Team with an aim to feedback to the source within two weeks of initial receipt of a feasibility request. Specific CRCI staff based in these units support Investigators with the rapid & accurate completion of the feasibility assessment and timely delivery of study start-up and first patient first visit (FPFV).

To place a study feasibility service request:

To place a study feasibility service request please email and include the following supporting information and documents:

  • Protocol synopsis
  • Study feasibility questionnaire (if available)
  • Study timelines, including accrual timelines (local and international)
  • Any specific trial related questions which are critical to evaluating feasibility (e.g. Standard treatments, study assessments etc.)
  • Confirm if the study is definitely being placed in Ireland, or if the applicant is currently bidding for the study
  • Confidential disclosure agreement (if available)
  • A list of potential sites (if available) and confirmation of which sites have been approached to date

To register as a potential investigator:

If you are a health care professional please register as a HRB CRCI investigator to participate in the HRB CRCI National Study Feasibility Programme. Investigator members are promptly informed of the latest research opportunities as they arise and can complete study feasibilities for studies of interest to them within their area of clinical interest.

To become a HRB CRCI Member:                Apply online

Study Feasibility Programme

For further information, or to discuss how we can assist you, please contact the central office
or email