SOCRA CCRP Exam Details & Actual Exam Questions
- Exam Code/Number: CCRP
- Exam Name/Title: Certified Clinical Research Professional (CCRP)
- Certification Provider: SOCRA
- Corresponding Certification: Clinical Research Professional
- Exam Questions: 132
- Updated On: Aug,31 2026
- Certification Level: Professional
SOCRA Certified Clinical Research Professional (CCRP) Exam Questions
View CCRP actual exam questions, answers and explanations for free.
94% student found the test questions almost same
All the information you need to pass SOCRA Certified Clinical Research Professional (CCRP) CCRP exam and free practice exam verified by EduDump exam experts.
Said the test questions were almost same
Passed the exams with the material
Found the study quides effective and helpful
(34 Up Votes)SOCRA CCRP Exam Overview:
| Certification Vendor: | SOCRA (Society of Clinical Research Associates) |
|---|---|
| Exam Name: | SOCRA Certified Clinical Research Professional Examination |
| Exam Number: | CCRP |
| Certificate Validity Period: | 3 years |
| Exam Format: | Multiple-choice questions, Computer-based testing, Remote live proctoring available |
| Exam Price: | $325 (SOCRA members) / $500 (non-members) |
| Passing Score: | 72/100 scored questions (~72%) |
| Exam Duration: | 210 minutes |
| Real Exam Qty: | 130 (100 scored, 30 unscored) |
| Available Languages: | English |
| Recommended Training: | SOCRA Training & Education SOCRA Official Study Materials |
| Exam Registration: | Prometric Scheduling SOCRA Official Registration |
| Sample Questions: | SOCRA CCRP Sample Questions |
| 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 |
|---|---|---|
| Study Close-Out and Post-Study Activities | 15% | - Archiving and retention of study records - Post-study responsibilities and follow-up - Study close-out procedures - Data management, analysis, and reporting - Final report preparation and submission |
| Research Study Implementation | 45% | - Investigational product management and accountability - Quality assurance and quality control - Adverse event reporting and safety management - Compliance with protocol, regulations, and GCP - Study conduct and monitoring activities - Data collection, source documentation, and CRF completion |
| Research Study Start-Up | 40% | - Institutional Review Board / Independent Ethics Committee (IRB/IEC) submission and approval - Informed consent process and documentation - Protocol development, review, and amendment - Regulatory requirements and guidelines (ICH-GCP, FDA, EMA, etc.) - Investigator and site qualification and selection - Regulatory document management and archiving |
0
0
0
10