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Introduction to Certified Clinical Research Associate Flashcards

7 cards from real CCRA practice questions. Tap to flip, then mark Knew It or Still Learning — missed cards come back until you master them.

Read the first 7 Introduction to Certified Clinical Research Associate flashcards as text
  1. Which organization administers the CCRA certification examination in the United States?

    Answer: The Association of Clinical Research Professionals (ACRP)

    ACRP (Association of Clinical Research Professionals) administers the CCRA certification exam and sets the competency standards for clinical research associates.

  2. A CRA notices that a site has been enrolling subjects without obtaining updated ICF signatures after a protocol amendment. What is the CRA's immediate obligation?

    Answer: Document the finding as a protocol deviation and report it to the sponsor

    Failure to obtain updated consent after an amendment is a protocol deviation that must be documented and reported to the sponsor per GCP guidelines.

  3. What does the term 'source document verification (SDV)' refer to in clinical monitoring?

    Answer: Comparing CRF data to original source documents to confirm accuracy

    SDV is the process of comparing data recorded in the CRF against original source documents to ensure data accuracy and integrity.

  4. Under 21 CFR Part 312, an Investigational New Drug (IND) application must be submitted to the FDA before:

    Answer: Initiating a clinical investigation of a new drug in humans

    An IND must be in effect before a sponsor ships an investigational drug across state lines or begins clinical studies in humans.

  5. Which ICH E6(R2) principle states that clinical trial information should be recorded, handled, and stored in a way that allows its accurate reporting, interpretation, and verification?

    Answer: Data integrity

    ICH E6(R2) emphasizes that all clinical trial data must be handled and stored to allow accurate reporting, interpretation, and verification.

  6. What is the primary purpose of a Clinical Study Report (CSR)?

    Answer: To provide a comprehensive integrated summary of the methods and results of a clinical trial

    A CSR is a comprehensive document integrating clinical and statistical descriptions and analyses of results, required for regulatory submissions.

  7. In risk-based monitoring (RBM), which factor is typically used to prioritize monitoring resources?

    Answer: The criticality of data and processes to subject safety and data integrity

    RBM prioritizes monitoring efforts based on the risk to subject safety and data integrity, focusing resources where they will have the greatest impact.

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Sources & references

Exam facts on this page (fees, format, dates, passing scores) are checked against these official sources; the date is our last check. Editorial policy

  1. acrpnet.org — Registration deadline, eligibility, fees, exam format, score release, test dates, time limit, score validity, registration, retake fee · verified Nov 2026
  2. test-takers.psiexams.com — Test delivery · verified Oct 2026