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Protocol Review Process

Prior to submitting your proposal involving cancer patients to the University of Pittsburgh Institutional Review Board (IRB)/PittPRO, you must submit it to and receive approval from the UPMC Hillman Cancer Center Protocol Review Committee/Protocol Review and Monitoring System (Hillman PRC/PRMS).

  • The Hillman PRC/PRMS meets twice per month to review new interventional proposals. View the meeting schedule.
  • Complete a PRC/PRMS Checklist Form to submit with your new study.
  • Your interventional proposal should include the following:
    • Completed PRC/PRMS checklist
    • Full, complete protocol and appendices
    • Summary or synopsis of protocol (optional)
    • Informed Consent form(s) (institution or sponsor’s consent forms)
    • Investigational drug brochure
    • Investigator-initiated study, including biostatistical approval
  • If your protocol is non-interventional, only need to provide the non-therapeutic # request form above, as well as protocol. This should be provided PRIOR to submission in PittPRO. Please also indicate the HCC# if making a submission in PittPRO.
  • Submit all documents electronically to:

    Brandon Kaukus, BS
    Sr. Research & Risk Mgmt Review Specialist
    Clinical Protocol and Data Management (CPDM)
    UPMC Cancer Pavilion
    5150 Centre Avenue, Suite 301
    Pittsburgh, PA 15232-1305
    Phone: 412-623-3376
    Email: kaukusbm@upmc.edu
    Fax: 412-648-6650

  • Results of the Hillman PRC/PRMS review will be sent to you approximately one week after the scheduled meeting.
    The committee may request additional information or clarifications to questions generated at the meeting. Please provide a prompt response to the committee’s comments so that your proposal can be approved quickly. Approval will not be granted until all questions/clarifications have been addressed and the committee has accepted the responses. Electronic submissions are preferred.

    Protocols do not require an annual review by the Hillman PRC/PRMS unless there are significant modifications to the study design.