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ACRP Certified Professional Sample Questions:
1. When designing a clinical trial, why is it important to define the study population?
A) To support subject recruitment to the study
B) To determine where to conduct the study
C) To determine the study objectives
D) To support the study objectives
2. A study is using an EDC system. After the data is entered into EDC, who is the next to review and conduct SDV of this data?
A) Monitor
B) Sponsor
C) Data Manager
D) QA Department
3. Who should vote during the IRB/IEC review and discussion process?
A) All IRB/IEC members
B) All IRB/IEC members and non-member experts
C) All members who were involved in the review and discussion
D) All members who were involved in the review and discussion and non-member experts
4. Which of the following is a conflict of interest for a PI conducting a study?
A) A PI that votes on the IRB/IEC approval of the protocol
B) A PI who is a key opinion leader, writes the protocol
C) A PI who receives payment for the study
D) A PI that presents at an investigator meeting
5. While reviewing a new protocol, a PI realizes a specialized laboratory test is required that the local hospital does not perform. The PI locates a laboratory that performs the specialized test and retains their services.
Responsibility for ensuring the laboratory retained is qualified for this trial-related task lies with the:
A) CRC
B) PI
C) Sponsor
D) CRO
Solutions:
| Question # 1 Answer: D | Question # 2 Answer: A | Question # 3 Answer: C | Question # 4 Answer: A | Question # 5 Answer: B |
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