Association of Clinical Research Professionals (ACRP) Certified Professional Practice Exam

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Prepare for the ACRP Certified Professional Exam with our comprehensive quiz. Elevate your clinical research skills with targeted flashcards and multiple-choice questions. Enhance your readiness with detailed explanations and insights for improved performance!

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During a multi-site clinical study, who is responsible for reporting the subject recruitment rate?

  1. The site investigator

  2. The Clinical Research Associate (CRA)

  3. The study sponsor

  4. The regulatory agency

The correct answer is: The Clinical Research Associate (CRA)

The responsibility for reporting the subject recruitment rate during a multi-site clinical study typically falls to the Clinical Research Associate (CRA). CRAs play a crucial role in monitoring the progress of clinical trials, including the recruitment of subjects. Their duties involve coordinating between multiple sites, ensuring compliance with the study protocol, and collecting relevant data on recruitment rates. This information is essential for the study’s timeline and for assessing whether the trial is progressing as planned. While site investigators are responsible for overseeing the recruitment at their specific sites, they typically report recruitment data to the CRA, who then compiles and communicates this information to the study sponsor. Thus, the CRA acts as a central point for consolidating recruitment data from various investigators and sites, ensuring a comprehensive overview of the study’s recruitment performance.

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