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Updated: Aug 13, 2026
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ACRP ACRP-CP Exam Overview:
| Certification Vendor: | Association of Clinical Research Professionals (ACRP) |
| Exam Name: | ACRP Certified Professional Exam |
| Exam Number: | ACRP-CP |
| Related Certifications: | ACRP Certified Clinical Research Associate (CCRA) ACRP Certified Clinical Research Coordinator (CCRC) ACRP Certified Principal Investigator (CPI) |
| Certificate Validity Period: | 3 years |
| Exam Format: | Multiple-choice questions, Recall questions, Scenario-based questions |
| Available Languages: | English |
| Exam Duration: | 180 minutes |
| Passing Score: | Scaled score of 600 or higher |
| Real Exam Qty: | 125 (100 scored, 25 pre-test) |
| Exam Price: | $435 – $600 |
| Recommended Training: | ACRP Official Training Resources |
| Exam Registration: | ACRP Official Registration |
| Sample Questions: | ACRP ACRP-CP Sample Questions |
| 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 |
|---|---|---|
| Clinical Study Operations | 15% | - Project management
|
| Data Management and Informatics | 17% | - Data reporting
|
| Study Design and Conduct | 17% | - Study planning
|
| Professionalism and Ethical Practice | 15% | - Continuous improvement
|
| Ethical and Participant Safety Considerations | 19% | - Ethical principles
|
| Regulatory and Compliance Requirements | 17% | - Compliance procedures
|
ACRP Certified Professional Sample Questions:
1. The IRB/IEC has decided to not approve a clinical trial. Who must they notify in writing?
A) Regulatory Agency
B) PI
C) CRC
D) Sponsor
2. The objective of a randomized clinical trial is to look at whether an IP is effective in preventing recurrence of a disease. What would be a possible primary endpoint of the trial?
A) Use of concomitant medications to treat the symptoms
B) Impact of an approved vaccine against the disease
C) Occurrence of known side effects of the IP
D) Time to occurrence of symptoms of the disease
3. A site is starting up a Phase III trial. They have received IRB/IEC approval and have scheduled the SIV. The site cannot begin enrolling subjects until:
A) The DSMB meets and the first DSMB meeting report has been issued.
B) A signed clinical trial agreement between the site and sponsor is in place.
C) The site receives approval from the medical monitor to begin enrolling.
D) The CRA has performed source document review and verification at the site.
4. Who should vote during the IRB/IEC review and discussion process?
A) All IRB/IEC members and non-member experts
B) All members who were involved in the review and discussion
C) All IRB/IEC members
D) All members who were involved in the review and discussion and non-member experts
5. Access to study documentation for auditors and inspectors during an audit or inspection at a clinical trial site is the responsibility of the:
A) PI
B) CRC
C) CRA
D) Sponsor
Solutions:
| Question # 1 Answer: B | Question # 2 Answer: D | Question # 3 Answer: B | Question # 4 Answer: B | Question # 5 Answer: A |
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