CCRA Introduction to Certified Clinical Research Associate 5

Question 1

Which of the following is a key difference between a CRA (Clinical Research Associate) and a CRC (Clinical Research Coordinator)?

Accepted Answer

A CRA is typically employed by the sponsor or CRO and monitors sites; a CRC works at the investigator site and supports trial conduct

Answer

CRAs are sponsor or CRO employees who monitor site compliance, while CRCs are site staff who assist investigators in day-to-day trial operations.

Question 2

What is the purpose of a Pre-Study Site Qualification Visit (SQV)?

Accepted Answer

To evaluate whether the site and investigator have the capabilities, resources, and patient population to conduct the trial

Answer

An SQV assesses the site's facilities, staff qualifications, patient access, and overall feasibility before committing to site selection.

Question 3

According to ICH E6(R2), what is meant by 'essential documents'?

Accepted Answer

Documents that individually and collectively permit evaluation of the conduct of a trial and the quality of the data produced

Answer

Essential documents are those that individually and collectively allow evaluation of the trial's conduct and data quality, and they form the Trial Master File.

Question 4

A sponsor is planning a multi-site trial across five countries. Which regulatory body's guidelines provide the internationally accepted standard for GCP that covers study design, conduct, performance, monitoring, and reporting?

Accepted Answer

ICH (International Council for Harmonisation) through Guideline E6

Answer

ICH E6 (Good Clinical Practice) is the internationally harmonized standard for the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials.

Question 5

What action should a CRA take if a site refuses to correct a major protocol deviation identified during a monitoring visit?

Accepted Answer

Escalate the issue to the sponsor's management and document the refusal in the monitoring report

Answer

When a site refuses corrective action, the CRA must document the refusal and escalate to sponsor management, who may involve regulatory authorities or terminate the site.

CCRA - Certified Clinical Research Associate Practice Test

CCRA - Certified Clinical Research Associate Practice Test

CCRA Introduction to Certified Clinical Research Associate 5