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!

Each practice test/flash card set has 50 randomly selected questions from a bank of over 500. You'll get a new set of questions each time!

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

The principal investigator
The clinical research coordinator
The CRA
The ethics committee

The correct answer is: The CRA

The clinical research associate (CRA) plays a key role in monitoring clinical trials, which includes tracking various metrics related to the study's progress, such as subject recruitment rates. The CRA is responsible for ensuring that the study adheres to regulatory requirements and protocols, and as part of this oversight, they compile and report data related to recruitment and retention of study subjects. While the principal investigator and clinical research coordinator may be involved in the day-to-day management and recruitment of subjects, the CRA's role specifically encompasses the broader oversight and reporting responsibilities to the sponsor and other stakeholders. The ethics committee focuses more on the ethical considerations of the study rather than its operational metrics like recruitment rates. Thus, the reporting of subject recruitment rates falls within the purview of the CRA's responsibilities, making them the appropriate choice for this question.