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Direct comparison

CIP vs CCRP Certification Compared

CIP (PRIM&R) certifies IRB/HRPP staff; CCRP (SOCRA) certifies clinical research conduct roles. Compare eligibility, exam cost, and career fit.

Side-by-side comparison

DimensionCIPCCRP
Full nameCertified IRB ProfessionalCertified Clinical Research Professional
Administered byCouncil for Certification of IRB Professionals (CCIP), under PRIM&RSOCRA (Society of Clinical Research Associates)
Established1999SOCRA founded 1991; first CCRP exam administered 1996
What it certifiesIRB/HRPP administration and oversightClinical trial conduct under GCP (coordinator + associate scope combined)
Typical role fitIRB coordinator, IRB administrator, HRPP director, compliance office staffClinical research coordinator or associate, site or sponsor/CRO staff
EligibilityBachelor's + 2 yrs HRPP experience (past 7 yrs), or 3 yrs experience without a degree3 pathways: 2 yrs experience (no degree required), OR CR degree + 1 yr, OR CR certificate + related degree + 1 yr
Exam format130 MCQ, 3 hours, in-person or live remote proctoring130 MCQ (100 scored + 30 unscored), Computer Based Testing only (since June 1, 2025)
Exam fee$425$510 members / $565 nonmembers (North America); $570 / $625 outside North America
Recertification cycleEvery 3 yearsEvery 3 years
CE requirementRecertification required every 3 yrs (CE set by CCIP/PRIM&R)45 CE hours per 3-yr cycle (22+ directly on CR regulations/policy) plus reapplication
Reflects ICH E6(R3)Not exam-content-specific to E6(R3)Yes, beginning the January 1, 2026 testing cycle

Common questions

FAQ

Is CIP or CCRP the right credential for an IRB coordinator?+

CIP. It is built specifically for IRB/HRPP office roles -- protocol review, meeting administration, and HRPP oversight -- while CCRP is built for clinical-trial-conduct roles running studies under IRB-approved protocols.

Is CIP or CCRP the right credential for a clinical research coordinator?+

CCRP (or ACRP's CCRC, a role-specific alternative). CCRP certifies the clinical-trial-conduct skill set -- consent, protocol adherence, source documentation, monitoring -- not IRB administration.

Can one person hold both CIP and CCRP?+

Yes -- eligibility and maintenance requirements for each are independent of the other. It is most common among professionals whose role spans both HRPP administration and clinical-trial-conduct functions.

Does either CIP or CCRP satisfy an FDA or ICH regulatory requirement?+

No. Neither the FDA nor ICH names CIP or CCRP as a required credential for any role. Both are voluntary professional certifications; institutions, sponsors, and CROs decide independently whether to require or prefer either.

Referenced across the research world

University of Cambridge logoColumbia University logoCrossref logoUniversity of Edinburgh logoHarvard University logoUniversity of Oxford logoPrinceton University logoStanford School of Medicine logoUniversity College London logoORCID logoUniversity of Cambridge logoColumbia University logoCrossref logoUniversity of Edinburgh logoHarvard University logoUniversity of Oxford logoPrinceton University logoStanford School of Medicine logoUniversity College London logoORCID logo
  • University of Cambridge logo
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