In 2026, a good purchase experience should be forgettable: quick, secure, and done. From choosing a version to downloading 132 CCRP practice questions, PracticeVCE keeps every step straightforward so your energy goes into studying.
SOCRA CCRP Exam Overview:
| Certification Vendor: | SOCRA (Society of Clinical Research Associates) |
|---|---|
| Exam Name: | SOCRA Certified Clinical Research Professional Examination |
| Exam Number: | CCRP |
| Available Languages: | English |
| Exam Format: | Multiple-choice questions, Remote live proctoring available, Computer-based testing |
| Passing Score: | 72/100 scored questions (~72%) |
| Real Exam Qty: | 130 (100 scored, 30 unscored) |
| Exam Duration: | 210 minutes |
| Certificate Validity Period: | 3 years |
| Exam Price: | $325 (SOCRA members) / $500 (non-members) |
| Recommended Training: | SOCRA Training & Education SOCRA Official Study Materials |
| Exam Registration: | SOCRA Official Registration Prometric Scheduling |
| Sample Questions: | DOWNLOAD DEMO |
| Exam Way: | Computer-based at Prometric test centers or remote live proctoring |
| Pre Condition: | Eligibility: 3,500 hours of clinical research experience in past 5 years; or 2,500 hours + 2 years part-time; or academic pathways with degree + 1–1.5 years experience |
| Official Syllabus URL: | https://www.socra.org/certification/ccrp-certification-exam/ |
SOCRA CCRP Exam Syllabus Topics:
| Section | Weight | Objectives |
|---|---|---|
| Research Study Start-Up | 40% | - Institutional Review Board / Independent Ethics Committee (IRB/IEC) submission and approval - Regulatory requirements and guidelines (ICH-GCP, FDA, EMA, etc.) - Regulatory document management and archiving - Informed consent process and documentation - Protocol development, review, and amendment - Investigator and site qualification and selection |
| Study Close-Out and Post-Study Activities | 15% | - Study close-out procedures - Final report preparation and submission - Post-study responsibilities and follow-up - Archiving and retention of study records - Data management, analysis, and reporting |
| Research Study Implementation | 45% | - Compliance with protocol, regulations, and GCP - Investigational product management and accountability - Quality assurance and quality control - Adverse event reporting and safety management - Study conduct and monitoring activities - Data collection, source documentation, and CRF completion |
Before You Start: SOCRA Certified Clinical Research Professional (CCRP) Answers
CCRP is passed with 72/100 scored questions (~72%), and the official exam fee is $325 (SOCRA members) / $500 (non-members). Fixing these numbers early helps you set a measurable practice target.
SOCRA Official Registration: register for CCRP
Prometric Scheduling: register for CCRP
The CCRP exam contains 130 (100 scored, 30 unscored) questions to complete in 210 minutes minutes. Rehearsing under the same limit on the PracticeVCE engine turns pacing into a trained habit.
SOCRA Official Study Materials: Visit official page
SOCRA Training & Education: Visit official page
Choose the version of SOCRA Certified Clinical Research Professional (CCRP) you want, one, two, or all three, add it to the cart, and complete payment through the secure Credit Card checkout. The download link then arrives by email within about a minute, so your study starts without wasted time.
The package includes 132 practice questions for the CCRP exam. The count is set through analysis of a large volume of data, so the set matches the scope of the real test without padding.
- Research Study Start-Up (40%)
- Research Study Implementation (45%)
- Study Close-Out and Post-Study Activities (15%)
Divide your time according to each topic's weight.
Payment runs through the Credit Card system, a globally used online payment network. We never share your personal information with third parties without your permission, and we never send spam, so your details stay where they belong.
Eligibility: 3,500 hours of clinical research experience in past 5 years; or 2,500 hours + 2 years part-time; or academic pathways with degree + 1–1.5 years experience
SOCRA Certified Clinical Research Professional (CCRP) Sample Questions:
A subject currently on a clinical trial was hospitalized for 2 days due to a SAE. The subject reported the hospitalization to the investigator at the next study visit. According to the ICH GCP Guideline, when should the investigator report the SAE to the sponsor?
- A. Immediately
- B. Within 7 working days
- C. Within 10 working days
- D. Within 15 working days
Correct Answer: A 🗳️
Explanation: Only visible for PracticeVCE members. You can sign-up / login (it's free).
Protocol increases drug dose by 20%. Baseline: 370 mg/m². New dose = ?
- A. 420 mg/m²
- B. 400 mg/m²
- C. 492 mg/m²
- D. 444 mg/m²
Correct Answer: D 🗳️
Explanation: Only visible for PracticeVCE members. You can sign-up / login (it's free).
According to ICH GCP, who besides the sponsor should approve the financial aspects of a clinical trial?
- A. Investigator/institution
- B. OHRP
- C. DSMB
- D. Regulatory authority
Correct Answer: A 🗳️
Explanation: Only visible for PracticeVCE members. You can sign-up / login (it's free).
In accordance with the ICH GCP Guideline, who is responsible for the accuracy, completeness, legibility, and timeliness of the data reported to the sponsor in the case report forms and in all required reports?
- A. The clinical investigator
- B. The quality control specialist
- C. The IRB/IEC coordinator
- D. The contract research organization monitor
Correct Answer: A 🗳️
Explanation: Only visible for PracticeVCE members. You can sign-up / login (it's free).
Which of the following adverse events occurring during a study of an investigational new drug would require the sponsor to notify the FDA as soon as possible but in no case later than seven calendar days after the initial receipt of the information?
- A. An infection not related to the investigational drug requiring hospitalization for antibiotic therapy
- B. Death due to disease progression, mentioned in the investigator's brochure
- C. Aplastic anemia requiring hospitalization, mentioned in the investigator's brochure
- D. Death as a result of arrhythmias (irregular heart rhythm), not mentioned in the investigator's brochure and thought to be related to the use of the drug
Correct Answer: D 🗳️
Explanation: Only visible for PracticeVCE members. You can sign-up / login (it's free).
1257 Customer Reviews
