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 Download a PDF of CCRP Benefits and Quick Facts Here
  • One certification, CCRP®, for clinical research professionals

  • No need to obtain multiple certifications when you transition to varying roles in the clinical research arena. The scope of the Certification Program is based on the principles of Good Clinical Practice, including the US Code of Federal Regulations, ICH GCP E6, and the Ethical Principles that guide clinical research ( Belmont report, Declaration of Helsinki and the Nuremberg Code. )
    One certification covers: human clinical research of pharmaceuticals, biologics, medical devices and behavioral research within the US or internationally.
  • Available to non-members and to members (to members at a reduced cost)

  • Available to all persons working in clinical research (whether they are independent or affiliated with research institutions, CROs, SMOs, sponsors, or government) including:
    • clinical investigators 
    • coordinators
    • data managers
    • monitors
    • auditors 
    • research nurses
    • pharmacists 
    • project managers
    • statisticians
    • IRB and regulatory staff
    • regulators and government investigators
    • other clinical research professionals
  • Administered independently by the Certification Committee

  • Applicants must meet eligibility criteria

  • Three year certification period

Why is Being Certified Important?