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CIP (Certified IRB Professional)

The Certified IRB Professional (CIP) credential is an individual professional certification, awarded by the Council for Certification of IRB Professionals (CCIP) under PRIM&R (Public Responsibility in Medicine and Research), that formally recognizes a person's broad working knowledge of Institutional Review Board (IRB) functions and Human Research Protection Program (HRPP) administration. It attaches to the individual who holds it, not to an institution or an IRB itself -- an institution cannot be 'CIP-certified,' only the staff who administer or oversee its IRB/HRPP can be. Eligibility requires either a bachelor's degree plus two years of relevant HRPP experience, or three years of relevant HRPP experience without a degree, accumulated within the past seven years; candidates sit a 130-question, three-hour, closed-book exam covering human-subjects-protection regulations and IRB operations, and must recertify every three years.

ByCASRAI Editorial Board
· Last updated 1 Sept 2026
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Examples

Worked examples

  • Is an instance

    A university IRB coordinator who has spent three years processing protocol submissions documents that experience and sits the CCIP's 130-question exam; passing lets her add the CIP designation to her title and to the IRB office's staff page as evidence of the office's professional-development standard.

  • Is an instance

    During a for-cause OHRP audit, a hospital's Human Research Protection Program points to its IRB administrator's CIP credential -- current, recertified within the last three years -- as part of demonstrating that the office is staffed by professionals independently verified against a national body of IRB knowledge, not solely trained in-house.

Counter-examples

Looks similar, but isn't

  • Not an instance

    A vendor's 'CIP' designation for information-governance staff (AIIM's Certified Information Professional) or a financial institution's 'CIP' for IRA-compliance staff (Ascensus's Certified IRA Professional, tested by FINRA) share the exact same three-letter acronym but are entirely unrelated credentials administered by unrelated bodies in unrelated fields -- neither substitutes for, nor has anything to do with, PRIM&R's Certified IRB Professional. A search for 'CIP certification' returns all of these plus a fourth, NERC's power-grid critical-infrastructure-protection standard, so the acronym alone never disambiguates which credential is meant.

  • Not an instance

    Completing CITI Program human-subjects-research training satisfies a regulatory qualification-by-training requirement for individual investigators and IRB staff, but it is not the CIP credential -- CITI completion is a training record with no eligibility bar, exam, or recertification cycle; CIP is a standalone certification with all three.

Editorial commentary

Not to be confused with: Certified Information Professional (AIIM International’s information-management credential), Certified IRA Professional (Ascensus/FINRA’s financial-services credential), or NERC’s power-grid Critical Infrastructure Protection standards — all share the same ‘CIP’ acronym but are unrelated credentials from unrelated fields. Also distinct from CPIA (Certified Professional in IACUC Administration), PRIM&R’s sibling credential for the animal-research oversight side rather than the human-subjects IRB side. This page covers the Certified IRB Professional (CIP) credential specifically.

The Certified IRB Professional (CIP) credential is awarded by the Council for Certification of IRB Professionals (CCIP), operating under PRIM&R (Public Responsibility in Medicine and Research), to individuals who administer or oversee the day-to-day work of an Institutional Review Board (IRB) or a broader Human Research Protection Program (HRPP). Established in 1999, it was one of the first individual professional certifications built specifically for research-ethics-oversight staff, predating CPIA (established 2007) by nearly a decade.

What the credential certifies

CIP certifies broad working knowledge of IRB/HRPP functions, including:

  • Human-subjects protection regulations — the Common Rule (45 CFR 46), FDA human-subjects regulations, and the ethical principles articulated in the Belmont Report that underlie them.
  • IRB review mechanics — how protocols move through exempt, expedited, and full-board review categories, continuing-review requirements, and reportable-event handling.
  • HRPP administration — Federalwide Assurance (FWA) recordkeeping, OHRP registration and liaison duties, and the broader institutional infrastructure an IRB operates within.
  • Informed consent — what a compliant informed consent process requires and how IRB staff evaluate it during review.

Eligibility, exam, and recertification

Candidates qualify under one of two paths within the past seven years: a bachelor’s degree plus two years of relevant HRPP experience, or three years of relevant HRPP experience without a degree. The exam itself is 130 objective, multiple-choice questions administered over three hours, covering human-subjects-protection regulation and IRB/HRPP operations; it is offered continuously via in-person or live remote proctoring rather than on fixed testing windows. As of this writing the exam fee is $425. Certification must be renewed every three years — a materially shorter cycle than CPIA’s five-year renewal, reflecting the two credentials’ independent administration despite their shared CCIP/PRIM&R parent body.

CIP vs. CPIA vs. AAHRPP: three different things people conflate

These three are often mentioned in the same breath but certify different things at different levels:

  • CIP — an individual credential for human-subjects IRB/HRPP staff. This page.
  • CPIA — an individual credential for the parallel animal-research oversight side (IACUC administration), not human subjects.
  • AAHRPP — an organizational accreditation of an institution’s entire Human Research Protection Program as a unit, not an individual’s knowledge or credential at all.

See CASRAI’s IRB Certification guide for a fuller walkthrough of how CIP, general IRB/CITI training, and AAHRPP accreditation relate as options for an institution or individual to pursue, and the CIP vs. CCRP Certification comparison for how CIP stacks up against the clinical-trial-conduct-focused CCRP credential specifically.

Related CASRAI resources

Frequently asked questions

Is CIP the same as a Certified Information Professional or Certified IRA Professional?

No. Those are unrelated credentials — one in information governance (AIIM), one in financial/IRA compliance (Ascensus/FINRA) — that happen to share the same three-letter acronym. Only PRIM&R’s CCIP-administered credential is the Certified IRB Professional discussed here.

Do I need a degree to become a CIP?

No. A bachelor’s degree shortens the required experience window to two years of relevant HRPP work; without a degree, three years of relevant experience is required instead, both within the past seven years.

How is CIP different from CPIA?

CIP certifies human-subjects IRB/HRPP staff; CPIA certifies the parallel role on the animal-research IACUC side. They are administered by the same parent body (PRIM&R’s CCIP) but are separate credentials with separate exams and different recertification cycles (three years for CIP, five for CPIA).

Does an IRB itself need to be CIP-certified?

No — CIP certifies individuals, not institutions or boards. An institution’s Human Research Protection Program as a whole can instead pursue AAHRPP accreditation, which is a separate, organizational-level review.

References

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