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Updated: Jun 17, 2026
No. of Questions: 127 Questions & Answers with Testing Engine
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ACRP Certified Professional Sample Questions:
1. A PI on a study is a regular member of the IRB/IEC. Which of the following statements is TRUE regarding their participation in the IRB/IEC discussion and deliberation?
A) They cannot be the PI on the clinical study due to conflict of interest.
B) They can attend the meeting and can vote/provide opinion on whether to approve the study.
C) They can attend the meeting, but should not vote/provide opinion on whether to approve the study.
D) They must recuse themselves from the meeting given their dual roles as IRB/IEC member and PI.
2. Centralized monitoring can:
A) Indicate the need to send monitors to perform onsite visits.
B) Confirm why sites are deviating from the protocol.
C) Enable appropriate stratification of subject enrollment.
D) Identify IP accountability and storage issues.
3. Which of the following statements accurately describes the responsibilities of stakeholders involved in the conduct of a clinical study?
A) The regulatory authority is responsible for assessing and approving the clinical study protocol and accompanying CRF prior to implementation.
B) The IRB/IEC is responsible for obtaining consent from all subjects in the clinical study.
C) The sponsor is responsible for overseeing any delegated activities to a CRO and ensuring that the delegation of these activities is documented.
D) The CRC is responsible for identifying the relationship of an SAE to the IP.
4. A study sponsor approaches a facility about participating in their research study. The study sponsor requires use of social media as its sole method of recruitment. The site knows their institutional IRB/IEC does not approve of social media recruiting. How should the site respond?
A) Use a central IRB/IEC.
B) Decline the study.
C) Rely on the sponsor to notify the IRB/IEC.
D) Recruit for the study without use of social media.
5. Which of the following activities would be undertaken by the sponsor to BEST ensure overall quality of the study data?
A) Ensure there is an accompanying written record that describes the consent process.
B) Develop a plan that describes the monitoring approach for a clinical study.
C) Ensure submission of a data management plan to the regulatory authorities.
D) Conduct annual reviews of the protocol and accompanying study documents.
Solutions:
| Question # 1 Answer: D | Question # 2 Answer: A | Question # 3 Answer: C | Question # 4 Answer: B | Question # 5 Answer: B |
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