Free CCRC Exam Prep
Certified Clinical Research Coordinator (CCRC)
Prepare for the CCRC exam without spending hundreds on expensive prep courses. Free study guides, practice questions, flashcards, and related exam resources.
Quick Facts
Buy on AmazonExplore More ACRP Clinical Research Certifications
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CCRC ACRP Clinical Research Certifications License: Complete Roadmap
Follow this path to organize your licensing and exam preparation
Review the Exam Content Outline (ECO/DCO)
Download the official CCRC Detailed Content Outline from ACRP and identify your knowledge gaps across all six domains.
Study ICH GCP E6(R3) and Key ICH Guidelines
Read ICH E6(R3) GCP thoroughly — it has controlled ACRP examinations since July 15, 2026. Also review E2A, E8(R1), and the Declaration of Helsinki.
Focus on High-Weight Domains
Prioritize Clinical Trial Operations (23%), Study/Site Management (22%), and Ethical/Participant Safety (19%) — these three domains make up 64% of the exam.
Practice Questions and Mock Exams
Take timed practice exams covering all six domains. Review wrong answers thoroughly and identify recurring weak areas.
Final Review and Exam-Day Prep
Do a comprehensive review of all domains, focus on weak areas, and familiarize yourself with PSI remote or in-person testing procedures.
Can You Take the CCRC Exam?
Check if you meet the basic eligibility requirements
- •3,000 verified hours of clinical research coordinator work experience
- •Up to 1,500 hours may be waived with completion of an ACRP-approved clinical research education program
- •Alternatively, hold an active ACRP certification or complete an approved education program
- •Submit application with CV/resume and employer verification during registration window
CCRC Quick Facts
Time to Get Licensed
3-6 months of focused study for most candidates
From start to license in hand
Exam Provider
PSI (remote proctored or in-person test centers)
Retake Policy
Candidates who do not pass may retest 60 days after the original appointment or in the next available testing window by paying the exam fee. After two unsuccessful attempts, a new full application and all current fees are required.
Total Cost Breakdown
Free CCRC Prep Tools
100+ Practice Questions
Practice by topic with detailed answer explanations
AI Tutor Explains Mistakes
Understand why answers are wrong, not just which ones
Updated for 2026
Review the latest update date on each resource
$0 Forever
Start without a credit card or trial
What You'll Study
18 chapters covering the exam topics in this guide
Chapter 1: Scientific Concepts and Research Design
3 sections
Chapter 2: Ethical Principles and Guidelines
3 sections
Chapter 3: IRB/IEC Oversight and Participant Safety
3 sections
Chapter 4: Participant Rights and Ethics
3 sections
Chapter 5: Product Development and Regulatory Framework
3 sections
Chapter 6: Investigational Product Accountability
3 sections
Chapter 7: Regulatory Submissions and Actions
3 sections
Chapter 8: Clinical Trial Operations and GCP Principles
3 sections
Chapter 9: Essential Documents and Site Qualification
3 sections
Chapter 10: Protocol Deviations and Amendments
3 sections
Chapter 11: Monitoring Visits and Audits
3 sections
Chapter 12: Study and Site Management - Startup
3 sections
Chapter 13: Enrollment and Recruitment
3 sections
Chapter 14: Daily Trial Coordination
3 sections
Chapter 15: Quality Improvement and Site Closeout
3 sections
Chapter 16: Source Documentation and Case Report Forms
3 sections
Chapter 17: Data Management and Queries
3 sections
Chapter 18: Data Privacy and Records Retention
3 sections
CCRC Exam Details
Certified Clinical Research Coordinator (CCRC)
Administered by ACRP (Association of Clinical Research Professionals)
Exam Content Breakdown
Based on the official ACRP (Association of Clinical Research Professionals) content outline
Protocol elements, study design, investigational brochures, research methodology, biostatistics, and clinical endpoints
Informed consent, IRB/IEC oversight, Declaration of Helsinki, adverse event reporting, vulnerable populations, and conflicts of interest
Drug and device development phases, regulatory submissions, investigational product accountability, labeling, and post-market requirements
ICH E6 GCP principles, protocol adherence, monitoring visits, essential documents, deviations, amendments, and quality management
Site startup and closeout, IP storage, budgets, contracts, equipment, staffing, enrollment management, and non-compliance
Source documentation, CRF/eCRF completion, data queries, electronic data capture, data privacy, and records retention
What's Included
18 Chapters
Complete exam coverage
Practice Quizzes
With detailed explanations
Free to Start
No credit card required
Quality Exam Prep Shouldn't Cost Hundreds
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What's Next After the CCRC?
After passing the CCRC, you can pursue these career paths
CCRA
Certified Clinical Research Associate — for professionals monitoring clinical trials at multiple sites
CPI
Certified Principal Investigator — for physicians and PIs leading clinical trial conduct
ACRP-CP
ACRP Certified Professional — broad clinical research certification for all roles
ACRP-MDP
ACRP Medical Device Professional — specialty credential for medical device clinical research
CCRC Exam FAQ
Official ACRP (Association of Clinical Research Professionals) Resources
Verify information with these official sources
More Free Resources
Ready to Start Your Free CCRC Prep?
Review the study guide, practice key concepts, and use the free tools at your own pace.