Facts verified Oct 16, 2026 against Academy of Clinical Research Professionals. Dates that have passed are removed automatically.
Facts verified Oct 16, 2026 against Academy of Clinical Research Professionals. Dates that have passed are removed automatically.
| 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.
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.
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.
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.
Interactive CCRC - Certified Clinical Research Coordinator resources on PracticeTestGeeks, free to start:
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.
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.
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.
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.
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?
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?
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?
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?
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