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ACRP Certified Professional Sample Questions:

1. An interim analysis is conducted during a clinical trial. To review the results, the sponsor assigns:

A) Investigators participating in the trial.
B) Executive board members.
C) Regulatory authority expert advisors.
D) Independent qualified individuals.

2. Which entity has ultimate responsibility over the conduct of the multi-center clinical trial?

A) CRO
B) Sponsor-Investigator
C) IRB/IEC
D) Regulatory authority

3. Which strategy is used to safeguard subject privacy?

A) Email updated enrollment logs to the CRA.
B) Store source documentation in the CRC's office.
C) Conduct subject-related conversations in controlled environments.
D) Utilize subject initials on correspondence.

4. Which of the following statements accurately describes the responsibilities of stakeholders involved in the conduct of a clinical study?

A) The CRC is responsible for identifying the relationship of an SAE to the IP.
B) The sponsor is responsible for overseeing any delegated activities to a CRO and ensuring that the delegation of these activities is documented.
C) The regulatory authority is responsible for assessing and approving the clinical study protocol and accompanying CRF prior to implementation.
D) The IRB/IEC is responsible for obtaining consent from all subjects in the clinical study.

5. All site financial matters pertaining to a trial are listed in what document?

A) Financial disclosure
B) Protocol
C) Signed contract
D) Informed consent form

Solutions: