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SOCRA CCRP Exam Overview:
| Certification Vendor: | SOCRA |
|---|---|
| Exam Name: | Certified Clinical Research Professional (CCRP) |
| Exam Number: | CCRP |
| Real Exam Qty: | 130 |
| Certificate Validity Period: | 3 years |
| Exam Duration: | 240 minutes |
| Related Certifications: | CCRP |
| Passing Score: | 71 |
| Available Languages: | English |
| Exam Price: | $510 - $625 USD |
| Exam Format: | Multiple Choice |
| Sample Questions: |  |
| Exam Way: | Computer Based Testing (CBT) at a testing center or Home Proctoring |
| Pre Condition: | Minimum two years of full-time employment (or 3500 hours of part-time employment) during the past five years as a clinical research professional OR a degree in 'Clinical Research' plus one year of experience. |
| Official Syllabus URL: | https://www.socra.org/certification/ccrp-certification-exam/exam-outline |
SOCRA CCRP Exam Syllabus Topics:
| Section | Weight | Objectives |
|---|---|---|
| Leadership and Professionalism | ||
| Research Study Conduct and Close-Out | ||
| Research Study Start-Up | 40% | - Coordinate the development of initial research study protocol
|
Everything You Wanted to Ask About the SOCRA Certified Clinical Research Professional (CCRP) Exam
Which domains make up the CCRP exam?
The SOCRA Certified Clinical Research Professional (CCRP) exam spans 3 domains, and they are not weighted equally. The top areas are Leadership and Professionalism, Research Study Conduct and Close-Out, Research Study Start-Up — 40%. Budget your study hours to match those weights; the full domain list is in the outline section further up this page.
What is the SOCRA Certified Clinical Research Professional (CCRP) exam, in plain terms?
The CCRP exam is SOCRA's official certification test, and passing it earns the Clinical Research Professional credential at the Professional level. In career terms, it is verified proof of skill — the kind that moves you up the shortlist when your company works with SOCRA technologies, or when you apply to one that does. The same track also includes CCRP, so this exam can anchor a longer certification plan.
What is the CCRP passing score, and how much is the exam fee?
You pass the SOCRA Certified Clinical Research Professional (CCRP) exam at 71, and each attempt costs $510 - $625 USD — fail, and that fee is due again in full for the retake. Treat mock exams as insurance: keep practicing with Real4test until your scores sit comfortably above 71 twice in a row, then schedule the real CCRP exam.
Can I check your CCRP questions before buying?
Please do. Real4test offers a free demo download for the SOCRA Certified Clinical Research Professional (CCRP) exam — grab it from the product page or leave your email and we will send it over. Purchases come with 365 days of free updates; after that year, extending the update service costs 50% of the original price in your member zone.
How many questions are in the CCRP exam and how long does it run?
The SOCRA Certified Clinical Research Professional (CCRP) exam packs 130 questions into 240 minutes. That ratio leaves almost no room for stalling, so time management is a trained skill, not luck. Our suggestion: rehearse full-length timed sessions in the Real4test engine, learn to park a question and return later, and walk into the CCRP exam with a pacing plan already rehearsed.
What are the eligibility requirements for the CCRP exam?
Minimum two years of full-time employment (or 3500 hours of part-time employment) during the past five years as a clinical research professional OR a degree in 'Clinical Research' plus one year of experience. Since SOCRA revises these rules from time to time, confirm the current prerequisites on the official exam page (https://www.socra.org/certification/ccrp-certification-exam/exam-outline) before booking your SOCRA Certified Clinical Research Professional (CCRP) exam.
What if I fail — and how fast is delivery?
Delivery is effectively instant: your CCRP download link is emailed within one minute of payment, with no cap on how many computers you install it on. If the email has not shown up within 2 hours, check spam and contact our 7x24 support — we reply quickly and resend immediately. If you fail the SOCRA Certified Clinical Research Professional (CCRP) exam itself, the refund policy applies when you took the corresponding exam within 60 days of purchase: submit a scanned enrollment slip and the official Score Report PDF within 2 days after the exam, and the refund is processed within 7 days. Not covered: attempts within 3 days of purchase, exams never actually taken, free materials, and expired orders — and the candidate name must match the payer name. Prefer material over money? Exchange for two free exam products of equal value and keep the update service on your original purchase.
SOCRA Certified Clinical Research Professional (CCRP) Sample Questions:
Question #1
Protocol increases drug dose by 20%. Baseline: 370 mg/m². New dose = ?
A. 492 mg/m²
B. 400 mg/m²
C. 420 mg/m²
D. 444 mg/m²
Question #2
In accordance with 45 CFR 46, in addition to the Office for Human Research Protections (OHRP), a suspension of IRB/IEC approval must be reported to which of the following?
A. The local hospital's medical director
B. The appropriate institutional officials
C. The Scientific Review Committee
D. The local hospital's bioethics committee
Question #3
In accordance with the CFR, for at least how many years after the completion of a study must the clinical investigator provide the sponsor with relevant changes to financial information?
A. One year
B. Three years
C. Five years
D. Two years
Question #4
A Phase I clinical trial is initiating. Who is responsible for ensuring that site staff are adequately informed about trial duties?
A. Program manager
B. Sponsor
C. Clinical investigator
D. IRB/IEC
Question #5
Which of the following is an adequate definition of quality assurance for the conduct of a clinical trial?
A. An official review by a regulatory authority of documents, facilities, records, and any other resources that are deemed to be related to the trial
B. The act of reviewing and approving the investigational protocol and informed consent document
C. The systematic plan to review, approve, and monitor biomedical and behavioral research involving human subjects
D. The planned and systematic actions established to ensure that the trial is performed and the data are generated, documented, and reported in compliance with GCP and the applicable regulatory requirements
Solutions:
| Question #1 Correct Answer: D | Question #2 Correct Answer: B | Question #3 Correct Answer: D | Question #4 Correct Answer: C | Question #5 Correct Answer: D |
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