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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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21. In a Phase III cardiovascular trial, who is responsible for ongoing clinical trial safety evaluation?
22. A study coordinator is developing an informed consent form for the first time.
23. A subject has creatinine 1.
24. Which of the following adverse events occurring during a study of an investigational new drug...
25. In accordance with ICH/GCP Guidance, how long should an IRB/IEC retain all relevant study-related records...
26. In accordance with the ICH GCP Guideline and the CFR, who is directly responsible for...
27. Which of the following is one of the responsibilities of an investigator?
28. A physician with 20 years of experience is planning to be the site investigator for...
29. Which of the following elements should NOT influence the investigator’s ability to obtain endpoint data?
30. An approved investigational device exemption (IDE) permits a device to be:
31. Which of the following statements about the initial IND application submission by a sponsor to...
32. Which of the following identifies content that should be included in a clinical research protocol?
33. Protecting prisoners’ rights to voluntarily participate in research is an example of which Belmont principle?
34. In accordance with the ICH E2A Guideline, the sponsor must report an adverse event that...
35. While reviewing site records during a monitoring visit, a monitor can cite which of the...
36. In accordance with 45 CFR 46, in addition to the Office for Human Research Protections...
37. During an audit for a Phase II IND study, the auditor identified unreported serious protocol...
38. Upon completion of a study, the investigator should do which of the following?
39. In accordance with the Belmont Report, obtaining voluntary informed consent from subjects prior to enrolling...

SOCRA CCRP Summary

  • Vendor: SOCRA
  • Product: CCRP
  • Update on: Nov 11, 2025
  • Questions: 130
  • Page: 2 / 2
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TESTED 11 Nov 2025