Exam Name: ACRP Certified Professional Exam
Certification Provider: ACRP
Corresponding Certification: ACRP Certified Professional
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Instant Download ACRP-CP Exam Dumps : ACRP Certified Professional Exam
Updated: Sep 21, 2026
No. of Questions: 127 Questions & Answers with Testing Engine
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A better life is built from better qualifications, and better qualifications are built from honest preparation. PassLeaderVCE handles the materials for the ACRP-CP exam: 127 practice questions, three formats, updates free for 365 days.
ACRP ACRP-CP Exam Overview:
| Certification Vendor: | Association of Clinical Research Professionals (ACRP) |
|---|---|
| Exam Name: | ACRP Certified Professional Exam |
| Exam Number: | ACRP-CP |
| Exam Duration: | 180 minutes |
| Passing Score: | Scaled score of 600 or higher |
| Related Certifications: | ACRP Certified Principal Investigator (CPI) ACRP Certified Clinical Research Associate (CCRA) ACRP Certified Clinical Research Coordinator (CCRC) |
| Exam Price: | $435 – $600 |
| Certificate Validity Period: | 3 years |
| Available Languages: | English |
| Real Exam Qty: | 125 (100 scored, 25 pre-test) |
| Exam Format: | Multiple-choice questions, Scenario-based questions, Recall questions |
| Recommended Training: | ACRP Official Training Resources |
| Exam Registration: | ACRP Official Registration |
| Sample Questions: | DOWNLOAD DEMO |
| Exam Way: | Online remote proctored or in-person at PSI test centers |
| Pre Condition: | 3,000 hours verifiable clinical research work experience; or 1,500 hours plus clinical research degree |
| Official Syllabus URL: | https://acrpnet.org/certification/acrp-cp-certification |
ACRP ACRP-CP Exam Syllabus Topics:
| Section | Weight | Objectives |
|---|---|---|
| Topic 1: Regulatory and Compliance Requirements | 17% | - International standards
|
| Topic 2: Clinical Study Operations | 15% | - Project management
|
| Topic 3: Data Management and Informatics | 17% | - Data collection
|
| Topic 4: Professionalism and Ethical Practice | 15% | - Continuous improvement
|
| Topic 5: Ethical and Participant Safety Considerations | 19% | - Safety monitoring and reporting
|
| Topic 6: Study Design and Conduct | 17% | - Study planning
|
Questions About the ACRP Certified Professional Exam, Answered
The official ACRP Certified Professional outline defines 6 domains. The leading three are Regulatory and Compliance Requirements (17%), Ethical and Participant Safety Considerations (19%), and Clinical Study Operations (15%). The full list is in the topics section above, and PassLeaderVCE's 127 practice questions cover each one.
The ACRP-CP exam is a ACRP certification exam validating the ACRP Certified Professional syllabus shown above. It belongs to these credential paths: ACRP Certified Clinical Research Associate (CCRA), ACRP Certified Clinical Research Coordinator (CCRC), ACRP Certified Principal Investigator (CPI). In a crowded 2026 job market, the credential demonstrates ability visibly — and PassLeaderVCE prepares candidates with 127 practice questions in PDF, Desktop Test Engine, and Online Test Engine formats.
PassLeaderVCE issues a full refund if you take the ACRP Certified Professional exam within 60 days of purchase and do not pass. The policy does not apply if the exam is taken within 3 days of purchase, if the exam was never actually taken, or to free materials or expired orders, and the candidate name must match the payer name. Submit a scan of your enrollment slip and the official Score Report PDF within 2 days of the exam; claims are processed within 7 days. Alternatively, exchange for two free exam products of equal value and keep your original update service. Orders arrive by email within 1 minute — contact support if nothing arrives within 2 hours.
Online remote proctored or in-person at PSI test centers Register for the ACRP Certified Professional exam through these official channels:
After booking, PassLeaderVCE delivers your practice questions within 1 minute — preparation starts the same day.
The ACRP Certified Professional exam requires Scaled score of 600 or higher to pass, and registration costs $435 – $600. A failed attempt means paying the same fee again — a readiness check with the PassLeaderVCE engines before booking is the cheaper option.
Three versions of the same study materials: a printable, expert-prepared PDF with free demo download and instant access; a Desktop Test Engine for Windows that simulates the real exam with two practice modes and works offline; and an Online Test Engine for any browser on Windows, Mac, Android, and iOS with test history and performance review. All 127 practice questions are identical across versions. Every purchase includes 365 days of free updates — pushed to you automatically whenever the bank is revised — plus a 50% renewal discount afterward and unlimited computer installations.
The ACRP Certified Professional exam contains 125 (100 scored, 25 pre-test) to complete within 180 minutes. Timed simulation in the PassLeaderVCE Desktop Test Engine teaches that rhythm before exam day does.
ACRP recommends these training resources for the ACRP Certified Professional exam:
Follow the training with steady self-testing — the 127 practice questions from PassLeaderVCE help you apply theory and fill any gaps the training leaves.
3,000 hours verifiable clinical research work experience; or 1,500 hours plus clinical research degree Since requirements change over time, confirm the latest on the official ACRP exam page before scheduling.
ACRP Certified Professional Sample Questions:
All site financial matters pertaining to a trial are listed in what document?
- A. Informed consent form
- B. Financial disclosure
- C. Protocol
- D. Signed contract
Correct Answer: D 🗳️
Explanation: Only visible for PassLeaderVCE members. You can sign-up / login (it's free).
The PI should ensure that source data is:
- A. Printed directly from the EMR.
- B. Accurately reflected in the eCRFs.
- C. On worksheets that are provided by the sponsor.
- D. Kept on site for a minimum of 2 years.
Correct Answer: B 🗳️
Explanation: Only visible for PassLeaderVCE members. You can sign-up / login (it's free).
An investigator in a multicenter trial reports multiple occurrences of an SAE to the sponsor. Who is responsible for reporting the SAEs to the remaining sites' IRB/IECs?
- A. Regulatory authority
- B. Original reporting investigator
- C. Investigator at each site
- D. Study sponsor
Correct Answer: D 🗳️
Explanation: Only visible for PassLeaderVCE members. You can sign-up / login (it's free).
One key attribute for good study documentation is that the data are contemporaneous, which refers to the practice of:
- A. Comparing source document data to other data recorded in the same study time period.
- B. Recording data on source documents at the time the data are collected during the conduct of the study.
- C. Allowing real-time access for data review in the eCRF.
- D. Recording the date and time each data element is entered onto the source document.
Correct Answer: B 🗳️
Explanation: Only visible for PassLeaderVCE members. You can sign-up / login (it's free).
Which of the following statements accurately describes the responsibilities of stakeholders involved in the conduct of a clinical study?
- A. The IRB/IEC is responsible for obtaining consent from all subjects in the clinical study.
- B. The CRC is responsible for identifying the relationship of an SAE to the IP.
- C. The regulatory authority is responsible for assessing and approving the clinical study protocol and accompanying CRF prior to implementation.
- D. The sponsor is responsible for overseeing any delegated activities to a CRO and ensuring that the delegation of these activities is documented.
Correct Answer: D 🗳️
Explanation: Only visible for PassLeaderVCE members. You can sign-up / login (it's free).
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