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SOCRA CCRP Questions & Answers - in .pdf

CCRP pdf
  • Total Q&A: 132
  • Update: Aug 20, 2026
  • Price: $59.99
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  • Vendor: SOCRA
  • Exam Code: CCRP
  • Exam Name: Certified Clinical Research Professional (CCRP)
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Complete SOCRA Recommended Syllabus.
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Exact SOCRA CCRP Exam Questions with Correct Answers, verified by Experts with years of Experience in IT Field.

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SOCRA CCRP Q&A - Testing Engine

CCRP Study Guide
  • Total Q&A: 132
  • Update: Aug 20, 2026
  • Price: $59.99
Testing Engine
  • Vendor: SOCRA
  • Exam Code: CCRP
  • Exam Name: Certified Clinical Research Professional (CCRP)
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SOCRA CCRP Exam Overview:

Certification Vendor:SOCRA (Society of Clinical Research Associates)
Exam Name:SOCRA Certified Clinical Research Professional Examination
Exam Number:CCRP
Exam Duration:210 minutes
Certificate Validity Period:3 years
Passing Score:72/100 scored questions (~72%)
Exam Price:$325 (SOCRA members) / $500 (non-members)
Available Languages:English
Real Exam Qty:130 (100 scored, 30 unscored)
Exam Format:Multiple-choice questions, Computer-based testing, Remote live proctoring available
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:

TopicDetails
Topic 1
  • Research Study Start-Up: This section of the exam measures the skills of Clinical Research Coordinators and covers the initial planning and setup of a clinical trial. It involves coordinating the development of the study protocol, ensuring it considers ethical guidelines and regulatory pathways like IND or IDE. It also includes creating essential study documents like informed consent forms and case report forms. The domain covers obtaining necessary approvals from stakeholders like the IRB and sponsor, selecting study sites, training staff, and ensuring the study's compliance with various laws. Additionally, it involves obtaining the research product and preparing all necessary tools and documentation for the study's commencement.|Research Study Implementation: This section of the exam measures the skills of Clinical Research Associates and covers the active management and execution of the clinical trial. It focuses on following the study protocol and standard operating procedures, managing the investigational product, and ensuring ongoing regulatory compliance. The domain includes identifying, documenting, and reporting any study anomalies such as adverse events or protocol deviations. It also involves managing subject recruitment, consent, and retention, as well as maintaining all study records and essential documents. Furthermore, it covers communicating with all study stakeholders and participating in study audits to ensure quality and adherence to regulations.
Topic 2
  • Research Study Closure: This section of the exam measures the skills of Clinical Research Coordinators and covers the activities required to properly conclude a clinical trial. It involves participating in the study closeout visit to verify documentation and account for the investigational product. The domain also includes developing and submitting final closure reports to the IRB, study sponsor, regulatory authorities, and clinicaltrials.gov. Finally, it covers the procedures for archiving study records.

Reference: https://www.socra.org/certification/ccrp-certification-exam/exam-overview/

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