SOCRA CCRP Exam 2024 Practice Questions Part 1, 2, 3, 4
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Course
SOCRA CCRP
Institution
SOCRA CCRP
This set of practice questions is designed to help you prepare for the SOCRA Certified Clinical Research Professional (CCRP) Exam in 2024. The questions cover a range of topics relevant to clinical research, including ethical considerations, regulatory guidelines, and best practices in clinical tri...
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, 1: What is the primary purpose of the SOCRA CCRP certification?
The primary purpose of the SOCRA CCRP certification is to recognize
individuals who have demonstrated proficiency and expertise in clinical
research, ensuring they meet professional standards for conducting clinical
trials.
2: What is the minimum eligibility requirement for taking the CCRP exam?
The minimum eligibility requirement for taking the CCRP exam is having at
least two years of full-time experience in clinical research or an equivalent
combination of education and experience.
3: How often is the CCRP exam administered?
The CCRP exam is administered multiple times throughout the year at various
locations and can also be taken online through remote proctoring.
4: What is the format of the CCRP exam?
The CCRP exam consists of 130 multiple-choice questions, and candidates
have three hours to complete it.
5: Which regulatory body?s guidelines are primarily tested in the CCRP exam?
The CCRP exam primarily tests knowledge of FDA regulations and ICH-GCP
(International Council for Harmonisation - Good Clinical Practice) guidelines.
6: What is the passing score for the CCRP exam?
The passing score for the CCRP exam is typically set at 72%, although this can
vary slightly based on the exam version.
7: Can you retake the CCRP exam if you do not pass on the first attempt?
Yes, candidates can retake the CCRP exam if they do not pass on the first
attempt, but they must wait a minimum of 30 days before retaking it.
8: What is a key responsibility of a clinical research professional?
A key responsibility of a clinical research professional is to ensure that clinical
trials are conducted ethically and in compliance with all regulatory
requirements.
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