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SOCRA Clinical Research Professional (CCRP) Free Practice Questions

Getting ready for your SOCRA Clinical Research Professional CCRP exam can feel like a big hurdle, right? Don't worry, we've got your back! Jump into our completely free CCRP practice questions - they're just like the real test, designed to help you get comfortable and pinpoint exactly what you need to study more. Let's get you feeling super confident for exam day!

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1. In accordance with the CFR, the IRB/IEC membership must have:
2. Protocol increases drug dose by 20%.
3. In accordance with the CFR, which body must determine that a study meets the criteria...
4. In accordance with the CFR, the sponsor (who is not a sponsor-investigator) is responsible for...
5. A company’s CEO wants to commercially promote a device under an IDE study.
6. In accordance with the CFR, for at least how many years after the completion of...
7. A research assistant on a study was recently promoted to a clinical research coordinator (CRC)...
8. According to the CFR and the ICH GCP Guideline, which of the following must be...
9. In accordance with the ICH GCP Guideline, prior to initiating a trial, which of the...
10. A clinical investigator received an honorarium from the sponsor of a covered study.
11. In a completed multi-site Phase I drug study using remote EDC, who ensures the system...
12. In accordance with the ICH GCP Guideline, when a sponsor transfers trial-related duties andfunctions to...
13. The FDA may propose to terminate an IND during a Phase I study if the...
14. For a Significant Risk device study, an investigator must report within 5 working days which...
15. According to the CFR and ICH GCP, an IRB/IEC must retain all relevant records for...
16. According to ICH GCP, an electronic data capture (EDC) system must:
17. In accordance with the ICH GCP Guideline, who is responsible for the accuracy, completeness, legibility,...
18. An investigator received an updated informed consent form (ICF) from the sponsor for a study...
19. A research site was invited to participate in an investigational drug study.
20. A study team is preparing to initiate a Phase II trial for a novel colon...

SOCRA CCRP Summary

  • Vendor: SOCRA
  • Product: CCRP
  • Update on: Nov 12, 2025
  • Questions: 130
  • Page: 1 / 2
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TESTED 12 Nov 2025