CCRC Practice Test PDF (Free Printable 2026)
Pass your CCRC exam on the first attempt. Practice questions with detailed answer explanations, hints, and instant scoring.
CCRC: upcoming dates and official changes
- Oct 20, 2026 – Dec 31, 2026: Early-bird registration for the spring 2027 CCRC testing window runs from October 20 to December 31, 2026. (Academy of Clinical Research Professionals)
- Jan 1, 2027 – Apr 30, 2027: Regular registration for the spring 2027 CCRC testing window runs from January 1 to April 30, 2027. (Academy of Clinical Research Professionals)
- Feb 15, 2027 – May 15, 2027: The spring 2027 testing window for the ACRP CCRC exam runs from February 15 to May 15, 2027. (Academy of Clinical Research Professionals)
- Jul 15, 2027 – Oct 15, 2027: The fall 2027 testing window for the ACRP CCRC exam runs from July 15 to October 15, 2027. (Academy of Clinical Research Professionals)
- Jul 15, 2026: From July 15, 2026, the ICH E6(R3) Guideline for Good Clinical Practice replaced E6(R2) as the GCP reference for all ACRP exams, including the CCRC. (Academy of Clinical Research Professionals)
Facts verified Oct 16, 2026 against Academy of Clinical Research Professionals. Dates that have passed are removed automatically.
- The ACRP CCRC exam has 125 multiple-choice questions. (Academy of Clinical Research Professionals)
- Candidates have 180 minutes to answer the 125 questions on the ACRP CCRC exam. (Academy of Clinical Research Professionals)
- CCRC candidates need a scaled score of at least 600, on a 200–800 scale, to pass the exam. (Academy of Clinical Research Professionals)
- The ACRP CCRC exam costs $435 for ACRP members and $485 for nonmembers at early-bird registration, or $460 and $600 at regular registration. The price includes a non-refundable application fee and the exam fee. (Academy of Clinical Research Professionals)
- A CCRC retest costs $300–$325 for ACRP members and $350–$400 for nonmembers, and candidates who retest in the next testing window pay only the examination fee. (Academy of Clinical Research Professionals)
- A candidate who fails the CCRC exam can retest 60 days after the original test appointment or during the next available testing window. (Academy of Clinical Research Professionals)
- The CCRC certification is valid for two years and must then be maintained through ACRP's Maintenance of Certification process. (Academy of Clinical Research Professionals)
- The ACRP CCRC exam is delivered by PSI, either in person at a test center or remotely with online proctoring. (Academy of Clinical Research Professionals)
- CCRC candidates need 3,000 hours of verifiable paid work experience in human subject research, and ACRP may grant one 1,500-hour waiver for an active ACRP certification or a qualifying education program. (Academy of Clinical Research Professionals)
Facts verified Oct 16, 2026 against Academy of Clinical Research Professionals. Dates that have passed are removed automatically.
CCRC Exam at a Glance
| Item | Detail | Official source |
|---|---|---|
| Number of questions | 125 multiple-choice questions | Academy of Clinical Research Professionals |
| Time limit | 180 minutes | Academy of Clinical Research Professionals |
| Passing score | Scaled score of 600 (scale 200–800) | Academy of Clinical Research Professionals |
| Exam fee | $435 member / $485 nonmember (early bird); $460 member / $600 nonmember (regular) | Academy of Clinical Research Professionals |
| Retake fee | $300–$325 members / $350–$400 nonmembers (exam fee only) | Academy of Clinical Research Professionals |
| Retake policy | Retest 60 days after the original appointment or in the next testing window | Academy of Clinical Research Professionals |
| Validity | 2 years | Academy of Clinical Research Professionals |
| Delivery | PSI test center or remote online proctoring | Academy of Clinical Research Professionals |
| Eligibility | 3,000 hours of verifiable work experience (one 1,500-hour waiver possible) | Academy of Clinical Research Professionals |
| Score release | Pass/fail on screen immediately; full PSI score report within 48 hours | Academy of Clinical Research Professionals |
| Next exam date (Fall 2027) | Fall testing window July 15 – October 15, 2027 | Academy of Clinical Research Professionals |
| Registration deadline (Spring 2027) | Regular registration January 1 – April 30, 2027 | Academy of Clinical Research Professionals |
| Registration opens (Spring 2027) | Early-bird registration October 20 – December 31, 2026 | Academy of Clinical Research Professionals |
| Testing window (Spring 2027) | February 15 – May 15, 2027 | Academy of Clinical Research Professionals |
Facts verified Oct 16, 2026 against Academy of Clinical Research Professionals. Dates that have passed are removed automatically.
CCRC Practice Test PDF – Free Printable Exam Prep
Preparing for the CCRC exam? A printable CCRC practice test PDF lets you review questions, test your knowledge offline, and build the exam readiness that timed, screen-based testing demands. Whether you are studying at home, commuting, or revisiting weak areas on paper, a printed practice test remains one of the most effective preparation formats available. This page provides a free PDF download and a structured study guide for the CCRC examination. Practice with the free CCRC - Certified Clinical Research Coordinator practice test on PracticeTestGeeks (7 questions with answer explanations).
The CCRC assessment tests candidates on the core competencies required for certification or qualification in the field. A strong preparation strategy combines repeated practice testing with targeted review of areas where accuracy falls below 70%. Use this PDF alongside the online CCRC practice tests on this site for the most complete preparation experience — paper for review and annotation, online for timed simulation with instant scoring.
What the CCRC Exam Covers
Candidates are tested across the primary knowledge domains that define competency in the CCRC field. Each domain contributes a weighted percentage of the total scored questions. High-weight domains deserve proportionally more preparation time. The exam format is typically multiple-choice, and understanding the question structure — identifying the best answer rather than the first correct-sounding one — is as important as content knowledge.
Common high-priority areas include foundational theory, applied practice, regulations or standards governing the field, and scenario-based reasoning that tests judgment under realistic conditions. Review official exam content outlines from the certifying body to confirm current domain weights before your examination date, as content outlines are updated periodically.
How to Use This Practice Test PDF
Print the PDF, set a timer proportional to the number of questions, and complete each section without reference materials to simulate real exam conditions. After grading, categorize every incorrect answer by domain to build a targeted error log. Prioritize re-study in your weakest domains, then take an additional timed practice session to confirm improvement. Repeat the cycle until accuracy is consistently above 75% across all domains.
Free CCRC - Certified Clinical Research Coordinator Study Tools
Interactive CCRC - Certified Clinical Research Coordinator resources on PracticeTestGeeks, free to start:
- CCRC - Certified Clinical Research Coordinator flashcards — review key terms and concepts card by card
- CCRC - Certified Clinical Research Coordinator study guide — topic-by-topic overview of what the exam covers
- CCRC - Certified Clinical Research Coordinator cheat sheet — one-page printable summary for last-minute review
Key Takeaway: CCRC certification demonstrates expertise in this field. Most candidates spend 4-8 weeks preparing with practice tests before taking the exam.

Study Strategy for the CCRC Exam
Build Your Content Foundation First
Before attempting practice tests, ensure you have reviewed the official study materials for the CCRC exam. Most certifying bodies publish a candidate handbook or content outline that lists exactly what knowledge is tested. Read this document first — it tells you not only what to study but also what to ignore. Allocate study time in proportion to domain weights: spend more time on high-weight domains and less on domains you already know well.
Practice Testing and Error Analysis
Once you have reviewed the content, move to practice testing. Each practice test session should be treated as a diagnostic: the questions you answer incorrectly are more valuable than the ones you answer correctly. Keep an error log organized by domain. After three to four practice tests, patterns in your errors will become clear. These patterns tell you exactly where to concentrate additional study effort.
Final Preparation Week
In the week before the CCRC exam, focus on review rather than new learning. Take one full-length timed practice test to confirm readiness, then spend the remaining days reviewing your error log and reinforcing the concepts behind your most common mistakes. Avoid cramming new material in the final 48 hours — consolidation of existing knowledge is more valuable at that stage than attempting to add new content.
- ✓Download and read the official CCRC candidate handbook or content outline
- ✓Identify exam domains and their approximate percentage weights
- ✓Complete a baseline practice test to establish your starting accuracy by domain
- ✓Build an error log: record every missed question by domain and reason for error
- ✓Study the highest-weight CCRC domain first to maximize score impact
- ✓Take a second timed practice test after two weeks of study to measure improvement
- ✓Review answer explanations for every incorrect response, not just the correct answer
- ✓Simulate exam conditions: no notes, timed, single sitting per practice session
- ✓Confirm exam registration, location, ID requirements, and permitted materials in advance
- ✓Complete a final full-length practice test in the week before your exam date
Free CCRC Practice Tests Online
After completing this PDF, take full online CCRC practice tests at CCRC practice test — instant scoring with explanations for every answer. Use both formats together: this PDF for offline review and annotation, the online tests for timed simulation with immediate feedback. Together they give you the most complete CCRC exam preparation available on a single platform.
Sample CCRC - Certified Clinical Research Coordinator Practice Questions
Try these questions from our free CCRC - Certified Clinical Research Coordinator practice tests. The correct answer and an explanation follow each question.
A participant returns a partially used bottle of an oral investigational drug at a routine study visit. According to good clinical practice, what is the CRC's primary responsibility regarding the returned product?
- A. Instruct the participant to take the remaining product home for proper disposal.
- B. Immediately dispose of the unused product in a standard biohazard container.
- C. Accurately count the returned units, document the quantity on the accountability log, and store it securely per sponsor/protocol instructions.
- D. Offer the unused product to another participant who may have lost their supply to prevent waste.
Answer: C. Accurately count the returned units, document the quantity on the accountability log, and store it securely per sponsor/protocol instructions.
The site must maintain complete accountability for the investigational product from receipt to final disposition. This includes documenting the exact quantity of product returned by the participant and storing it securely. This process is crucial for assessing compliance and ensuring a complete reconciliation of all IP units at the end of the study, which are then either returned to the sponsor or destroyed according to the sponsor's specific written instructions.
A monitor is conducting source data verification (SDV) and notes that a blood pressure reading of '130/85' recorded in the electronic Case Report Form (eCRF) does not match the value of '135/80' written in the participant's original, signed progress note. This discrepancy is a violation of which core ALCOA-C principle of good documentation practice?
- A. Contemporaneous
- B. Accurate
- C. Legible
- D. Attributable
Answer: B. Accurate
The principle of "Accurate" documentation requires that the data recorded is a correct reflection of the source information. In this case, the discrepancy between the eCRF and the source document (the progress note) means the transcribed data in the eCRF is not accurate. The other principles, while important, do not directly address the correctness of the transcribed data.
A CRC measures a participant's blood pressure and immediately records the value, along with the time, date, and their initials, on the designated paper source worksheet. This practice best exemplifies which principle of ALCOA-C?
- A. Attributable
- B. Legible
- C. Contemporaneous
- D. Accurate
Answer: C. Contemporaneous
The principle of 'Contemporaneous' requires that data be recorded at the time it is generated or observed. By documenting the blood pressure reading immediately after taking it, the CRC ensures the record reflects the real-time event, preventing errors from recall. While the initials make it 'Attributable' and the value should be 'Accurate', the act of recording it *immediately* is the key to it being 'Contemporaneous'.
A participant has been enrolled in a long-term oncology trial for two years. The sponsor issues a protocol amendment that introduces a new, optional sub-study involving additional blood draws to test for a novel biomarker. What is the CRC's responsibility regarding the informed consent for this change?
- A. Obtain verbal consent from the participant for the sub-study and document it in the progress notes.
- B. No action is needed as the main study consent covers minor additions.
- C. Inform the participant of the new sub-study during their next visit without requiring a signature.
- D. Ensure the participant is re-consented using a new, IRB-approved consent form that details the optional sub-study.
Answer: D. Ensure the participant is re-consented using a new, IRB-approved consent form that details the optional sub-study.
Significant new information, such as additional procedures or changes in risk, requires that participants be re-consented. The CRC must use a revised, IRB-approved informed consent form to explain the changes and document the participant's willingness to continue in the trial under the new conditions.
Take the full CCRC - Certified Clinical Research Coordinator practice test
How this page was made: written with AI tools and published by Nathan Beja, founder of Practice Test Geeks, who is responsible for its content. Exam facts are checked against the official sources listed below. Not reviewed by a subject-matter expert. Editorial policy
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
- acrpnet.org — Eligibility, fees, exam format, score release, time limit, score validity, renewal, retake fee, retake policy, test delivery · verified Nov 2026