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      • Adult CIRB - Late Phase Emphasis Members
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    • Overview of the Study Review Process
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  • For Institutions
    • IRBManager Basics
    • Overview of the Study Review Process
    • Becoming A Signatory Institution
    • Navigating The CIRB For NCI Division of Cancer Prevention (DCP) Consortia Sites And Cancer Prevention Clinical Trial Network (CP-CTNET) Organizations
    • Create and Update the Signatory Institution Worksheet
      • Completing The Annual Signatory Institution Worksheet
      • Establishing Your Signatory Institution
      • Short Form Q & A
    • Creating and Updating the Annual Principal Investigator Worksheet
      • Establishing a Principal Investigator
    • How to Open a Study
      • Opening a Study
    • Change the PI on a Study
      • Changing the PI on a Study
    • Submit a Study Closure
    • Report A Potential Unanticipated Problem Or A Serious Or Continuing Noncompliance
    • Request an Assent Waiver
      • Completing The Assent Waiver Worksheet
    • Notify the CIRB about the participation of an incarcerated participant
      • Completing The Notification of Incarcerated Participant Worksheet
      • Institution Q & A
      • Boilerplate Language Q & A
      • Finding Information Q & A
      • Guidelines For Permitted Boilerplate Language Additions
      • Individual Roles Within The CIRB
      • Institutions' Roles With The CIRB
      • Managing Your CTEP Registration
      • Oversight Q & A
      • Updating Your CIRB Institution Roster using RUMS
      • Updating Your CIRB Person Roster using RUMS
      • Viewing Your CIRB Roster
  • For Networks
    • Overview of the Study Review Process
    • CIRB Document Posting
    • Submitting Studies
      • Completing The Translation Application
      • Completing The Unanticipated Problem And/Or Serious or Continuing Noncompliance Submission Application
      • Completing The Waiver Of Consent Application
      • Completing the Amendment Review Application
      • Completing the Continuing Review Application
      • Completing the Initial Review Application
      • Determining Waiver Of Consent Requirements
      • End User Licensing Agreement (Eula) Consent Form Language Q & A
      • Review of Translated Consent Forms, PROs, and Other Patient-Facing Documents
      • Submitting Recruitment/participant Materials For Review
    • CIRB Meeting Schedules
  • For Board Members
    • Become A Board Member
    • Overview of the Study Review Process
    • Resources
      • Helpful URLs
      • IRBManager Training for Board Members
    • CIRB Meeting Schedules
  • Contact Us

AIS Cancer Center at San Joaquin Community Hospital

  • Read more about AIS Cancer Center at San Joaquin Community Hospital

Cayuga Medical Center

  • Read more about Cayuga Medical Center

ECU Health Oncology-Kinston

  • Read more about ECU Health Oncology-Kinston

Jupiter Medical Center

  • Read more about Jupiter Medical Center

VA Southern Nevada Healthcare System

  • Read more about VA Southern Nevada Healthcare System

Denver Health Hospital Authority

  • Read more about Denver Health Hospital Authority

Oklahoma City VA Health Care System (VA Medical Center)

  • Read more about Oklahoma City VA Health Care System (VA Medical Center)

Mary Lanning Healthcare

  • Read more about Mary Lanning Healthcare

Robert J Dole VAMC

  • Read more about Robert J Dole VAMC

Individual Roles Within The CIRB

This Quickguide describes the four important roles at Institutions using the CIRB as their IRB of record.

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The NCI Central Institutional Review Board

401 N. Washington Street, Ste. 700
Rockville, MD 20850

The Central Institutional Review Board for the National Cancer of Institute is fully accredited by the Association for the Accreditation of Human Research Protection Program, Inc.