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Quizzes > Health & Medicine

What Is CCRP Quiz: Certified Clinical Research Professional

Quick, free CCRP certification quiz to test your knowledge. Instant results.

Editorial: Review CompletedCreated By: Ims AliUpdated Aug 26, 2025
Difficulty: Moderate
2-5mins
Learning OutcomesCheat Sheet
Paper art quiz illustration showing exam essentials icons and pass rate chart on golden yellow background for CCRP challenge

This quiz helps you confirm what CCRP means and how it applies to clinical research work. Practice key terms, ethics, and regulations in short items, then see where to review before the SOCRA exam. If you want more context on research standards, try our gcp quiz, or explore another acronym with the what does crcst mean guide.

Easy
What does the abbreviation CCRP stand for in clinical research?
Certified Clinical Review Practitioner
Certified Clinical Research Professional
Clinical Company Regulation Program
Clinical Compliance Research Protocol
CCRP stands for Certified Clinical Research Professional, a certification granted by the Society of Clinical Research Associates (SoCRA) to individuals who demonstrate competency in clinical research practice. Earning the CCRP credential validates proficiency in regulations, ethics, and trial conduct. It is widely recognized as a mark of quality in the industry.
Which organization offers the CCRP certification?
Association of Clinical Research Professionals (ACRP)
Society of Clinical Research Associates (SoCRA)
Food and Drug Administration (FDA)
World Health Organization (WHO)
The Society of Clinical Research Associates (SoCRA) administers the CCRP certification, setting standards and providing the exam for clinical research professionals. ACRP offers the CCRC credential instead. The FDA and WHO are regulatory/guideline bodies, but they do not issue the CCRP.
Which of the following is a primary benefit of holding a CCRP certification?
Grants automatic FDA approval for studies
Demonstrates professional competency in clinical research
Exempts from all regulatory audits
Allows unlimited research funding
CCRP certification demonstrates that an individual has met standards of knowledge and competency in clinical research, including regulations and ethics. It does not grant funding, approvals, or audit exemptions. Employers and sponsors often value CCRP-certified staff for quality assurance.
What is the minimum amount of professional clinical research experience required to be eligible for the CCRP exam?
Three months of part-time work
One year of internship experience
Two years of full-time clinical research experience
Four years in any healthcare field
SoCRA requires candidates to have at least two years of full-time professional experience in clinical research. Shorter internships or unrelated healthcare roles do not meet the eligibility. This ensures that applicants have practical exposure before certification.
Medium
How many total questions are included on the CCRP certification exam?
100 total questions (80 scored + 20 pilot)
200 total questions (175 scored + 25 unscored)
250 total questions (225 scored + 25 unscored)
150 total questions (all scored)
The CCRP exam consists of 200 questions: 175 are scored and 25 are unscored pretest items. This structure allows SoCRA to pilot new questions while maintaining a consistent scoring pool. Candidates should answer all items within the allotted time.
What is the minimum passing score for the CCRP examination?
85%
75%
55%
65%
Candidates must achieve a minimum of 65% correct responses on the scored items to pass the CCRP exam. This threshold reflects SoCRA's standard for demonstrating adequate competence. Scores are reported immediately after completion.
Which of the following domain areas is part of the CCRP exam blueprint?
Informed Consent and Human Subject Protection
Hospital Billing Procedures
Device Engineering Specifications
Pharmacy Dispensing Practices
The CCRP exam blueprint includes topics such as informed consent and human subject protection, clinical trial operations, and regulatory compliance. Pharmacy dispensing or billing procedures are not part of the clinical research domains tested. The blueprint ensures coverage of core research competencies.
How much time is allocated for candidates to complete the CCRP exam?
Two hours
Four hours
Three hours
One and a half hours
Candidates are given three hours (180 minutes) to complete all 200 questions on the CCRP exam. This time frame balances thorough assessment with practical scheduling. Adequate time management during the exam is critical.
Hard
How many continuing education (CE) credits are required to maintain CCRP certification every three years?
30 CE credits
20 CE credits
45 CE credits
60 CE credits
SoCRA requires CCRP holders to earn 45 CE credits within each three-year certification cycle to ensure ongoing competency. These credits can be obtained through workshops, conferences, or online courses approved by SoCRA. Failure to meet this requirement results in decertification.
Which of the following best describes the role of an Institutional Review Board (IRB) in clinical research?
Protects the rights and welfare of research participants
Manufactures investigational drugs
Markets approved pharmaceuticals
Sponsors and funds clinical trials
An IRB is an independent committee tasked with reviewing research protocols to safeguard the rights, safety, and welfare of human participants. It does not produce drugs, sponsor studies, or market products. IRB approval is mandatory before trials can begin.
What is the approximate first-time pass rate for the CCRP exam according to SoCRA statistics?
90%
50%
65%
80%
Historical data from SoCRA indicate that roughly 65% of candidates pass the CCRP exam on their first attempt. This pass rate underscores the exam's rigor and the need for thorough preparation. Preparation resources include study guides, practice tests, and SoCRA's workshops.
Where can candidates find the official CCRP exam content outline and test specifications?
On ClinicalTrials.gov
On the SoCRA website under certification resources
On the FDA's CFR database
On the WHO guidelines portal
SoCRA publishes the official exam content outline and test specifications on its website, under the certification resources section. This outline details domain weightings, topic areas, and sample questions. Other regulatory or guideline sites do not host SoCRA's specific exam blueprint.
Expert
Which international guideline is most frequently referenced in the CCRP exam for Good Clinical Practice standards?
ICH E6(R2) Good Clinical Practice
FDA 21 CFR Part 11
45 CFR Part 46
Declaration of Helsinki
The CCRP exam heavily references ICH E6(R2) Good Clinical Practice, which harmonizes international ethical and quality standards for clinical trials. While FDA and U.S. regulations and the Declaration of Helsinki are important, ICH E6(R2) serves as the primary global standard. Understanding its principles is critical for test success.
0
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Study Outcomes

  1. Define CCRP Certification -

    Understand what is CCRP, including its objectives and role in clinical research accreditation.

  2. Interpret SOCRA Exam Pass Rates -

    Analyze the latest socra exam pass rate statistics to gauge exam difficulty and candidate success factors.

  3. Evaluate Certification Value -

    Assess if ccrp certification is worth it by weighing its professional benefits against preparation commitments.

  4. Apply Core CCRP Concepts -

    Practice with ccrp test questions that reinforce foundational knowledge and exam essentials.

  5. Identify Exam Readiness -

    Determine your preparedness by pinpointing strengths and areas for improvement before the CCRP exam.

Cheat Sheet

  1. Core CCRP Exam Domains -

    What is CCRP? It covers five core domains: Ethics and Participant Protections, GCP, Regulatory Requirements, Study Operations, and Data Management, as defined by SOCRA and ACRP. Remember the mnemonic "Every Good Research Study Delivers" to lock in Ethics, GCP, Regulations, Study Ops, and Data.

  2. Key Regulatory Frameworks -

    Mastering 21 CFR Part 11 and ICH GCP guidelines is crucial for any CCRP test taker, as these set standards for electronic records and clinical trial conduct. A quick tip: "11 = Electronic" cements Part 11's focus on e-record compliance from FDA and ICH sources, boosting your confidence on exam day.

  3. Basic Sample Size Formula -

    Understanding n = (Z·σ/E)² is a must for hypothesis-driven trials; for a 95% confidence interval use Z = 1.96 and estimate σ from pilot data. Practice with σ = 10 and margin E = 2 to get n ≈ 96, reinforcing key statistical concepts with real numbers.

  4. Adverse Event Reporting -

    Regulations require reporting serious adverse events within 24 hours to both sponsor and IRB, per FDA guidelines (21 CFR 312.32). Use the mnemonic "SAE in a Day" (Serious - Alerts - Expedited - 24 hours) to keep timelines front and center.

  5. Evaluating SOCRA Exam Pass Rate -

    The latest SOCRA exam pass rate hovers around 70% according to the official SOCRA website, making this CCRP certification goal very achievable with solid prep. If you're asking "is CCRP certification worth it," remember that a strong pass rate translates to enhanced career credibility and growth in clinical research.

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