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ACRP Certified Professional Sample Questions:

1. A clinical trial where participants will be randomized to receive a sequence of two medications has which design configuration?

A) Parallel Group
B) Group sequential
C) Factorial
D) Crossover

2. The CRC is prepared to consent a cognitively impaired participant to an Alzheimer's clinical trial. The CRC is required to utilize which of the following in the consent process?

A) A member of the research team
B) A family member
C) A legally acceptable representative
D) A witness

3. A quality assurance audit of the EDC system SOP revealed a deficiency. Which of the following is the MOST likely reason?

A) The number of users with access was not defined.
B) The frequency of data backup was not defined.
C) The list of comparable technology solutions was not included.
D) The number of unique eCRF templates was not specified.

4. In order to conduct open-label, parallel group clinical trials according to sound scientific principles, which of the following design elements should be included?

A) Blinding
B) Privacy controls
C) Randomization
D) Placebo-controlled

5. Who determines what criteria and procedures should be followed if a subject discontinues/withdraws their consent?

A) Subject
B) CRO
C) Sponsor
D) PI

Solutions: