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ACRP Certified Professional follows objectives published by ACRP, so preparation should stay aligned with the official outline. Actual4dump organizes 127 ACRP-CP practice questions around those exam areas to support focused review.

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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
Real Exam Qty:125 (100 scored, 25 pre-test)
Exam Duration:180 minutes
Related Certifications:ACRP Certified Clinical Research Associate (CCRA)
ACRP Certified Principal Investigator (CPI)
ACRP Certified Clinical Research Coordinator (CCRC)
Passing Score:Scaled score of 600 or higher
Available Languages:English
Exam Price:$435 – $600
Certificate Validity Period:3 years
Exam Format:Multiple-choice questions, Recall questions, Scenario-based 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:

SectionWeightObjectives
Topic 1: Regulatory and Compliance Requirements17%- International standards
  • 1. Declaration of Helsinki
- ICH Guidelines
  • 1. E6(R2)/E6(R3) Good Clinical Practice
  • 2. E9 Statistical Principles
  • 3. E2A Expedited Reporting
  • 4. E11 Pediatric Trials
  • 5. E8 General Considerations for Clinical Trials
- Compliance procedures
  • 1. Regulatory submissions and approvals
  • 2. Audits and inspections
Topic 2: Clinical Study Operations15%- Site management
  • 1. Site personnel training and delegation
  • 2. Study documentation and record keeping
- Project management
  • 1. Vendor and stakeholder management
  • 2. Timeline and budget management
Topic 3: Study Design and Conduct17%- Study planning
  • 1. Sample size and statistical considerations
  • 2. Protocol development and amendments
  • 3. Study population and eligibility criteria
- Study implementation
  • 1. Investigational product management
  • 2. Study monitoring and oversight
  • 3. Site selection and activation
Topic 4: Ethical and Participant Safety Considerations19%- Ethical principles
  • 1. Human subject protections and privacy
  • 2. Clinical equipoise and therapeutic misconception
- Safety monitoring and reporting
  • 1. Adverse event identification and classification
  • 2. Safety information evaluation and communication
- Clinical care and management of research participants
  • 1. Standard of care vs protocol requirements
  • 2. Informed consent development and review
  • 3. Continuity of medical care
Topic 5: Professionalism and Ethical Practice15%- Continuous improvement
  • 1. Professional development and education
  • 2. Quality assurance and process improvement
- Professional standards
  • 1. Confidentiality and conflict of interest
  • 2. Role responsibilities and boundaries
Topic 6: Data Management and Informatics17%- Data collection
  • 1. Electronic data capture systems
  • 2. Case report form design and completion
- Data reporting
  • 1. Data integrity and security
  • 2. Database lock and data transfer
- Data quality control
  • 1. Query management and resolution
  • 2. Data validation and cleaning

ACRP ACRP-CP Exam Questions Answered

The ACRP-CP exam leads to the ACRP Certified Professional certification from Association of Clinical Research Professionals (ACRP). It is positioned at the Professional level. The exam validates the knowledge and skills expected of candidates preparing for ACRP Certified Professional.

Related certifications include:

  • ACRP Certified Clinical Research Associate (CCRA)
  • ACRP Certified Clinical Research Coordinator (CCRC)
  • ACRP Certified Principal Investigator (CPI)

The ACRP-CP exam includes 125 (100 scored, 25 pre-test) questions and allows 180 minutes. Before test day, divide the available time by the number of questions in a timed practice set to establish a steady per-question pace. If a difficult item starts consuming too much time, mark it for review and move forward instead of losing momentum. A full timed practice session can help you decide when to move on, when to return, and how much buffer to reserve for a final check.

The passing score for ACRP-CP is Scaled score of 600 or higher, and the official exam fee is $435 – $600. Because a retake requires paying the exam fee again, use timed practice results as a readiness check before scheduling your next attempt. If your performance remains inconsistent, continue reviewing weak domains and repeat a timed session before booking the exam.

3,000 hours verifiable clinical research work experience; or 1,500 hours plus clinical research degree

Eligibility rules can change, so confirm the current requirements on the official exam page before registering.

You can register through the official channels listed below:

The available exam delivery method is Online remote proctored or in-person at PSI test centers.

The official training options include:

After reviewing the recommended training, reinforce what you learned with Actual4dump's 127 practice questions for ACRP-CP.

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If you purchase the corresponding ACRP-CP preparation material and do not pass that exam within 60 days of purchase, you may apply for a full refund under the 100% Money Back Guarantee. The request requires a scanned exam enrollment slip and the official Score Report PDF, submitted within two days after the exam. Eligible requests are processed within seven days.

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The current ACRP-CP outline is organized into 6 top-level domains. The first listed areas include:

  • Professionalism and Ethical Practice (15%)
  • Study Design and Conduct (17%)
  • Data Management and Informatics (17%)

Review the Exam Topics section above for the complete outline and any nested subtopics.

ACRP Certified Professional Sample Questions:

Question 1

Preliminary evidence suggests a low-dose anti-cancer drug given for a short period of time may reduce the risk of developing cancer in patients who are at increased risk for developing cancer. The drug has potentially serious side effects. What is the MOST important question to consider before designing a clinical trial to test this hypothesis?

A. How effective is the drug at treating patients that have been previously diagnosed with cancer?
B. How willing are current patients to participate in a trial with potentially serious side effects?
C. How likely are patients at high risk of cancer going to develop cancer during the study?
D. How does the risk of developing cancer compare to the anticipated side effects from the drug?


Question 2

The IRB/IEC has decided to not approve a clinical trial. Who must they notify in writing?

A. CRC
B. Regulatory Agency
C. PI
D. Sponsor


Question 3

Who is responsible for securing agreement from all involved parties to ensure direct access of all trial-related source documents?

A. CRC
B. CRO
C. Investigator
D. Sponsor


Question 4

Who ensures information regarding payments to subjects is documented in a written consent form?

A. IRB/IEC
B. PI
C. Sponsor
D. Coordinator


Question 5

A study protocol must contain which of the following elements?

A. Description of statistical methods
B. Chemical structure of the IP
C. Participant reimbursement details
D. Data management plan


Solutions:

Question 1
Answer: D
Question 2
Answer: C
Question 3
Answer: D
Question 4
Answer: A
Question 5
Answer: A

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