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Clinical Research Associate Mock Interview

Question 2 of 40 for our Clinical Research Associate Mock Interview

Clinical Research Associate was updated by on May 22nd, 2023. Learn more here.

Question 2 of 40

What is your experience with following procedure, preparing for, and being involved in a regulatory audit and/or inspections of any kind?

"I have prepared for a Clinical Laboratory Improvement Amendments (CLIA) inspection by closely following all protocols while having good documentation practices. In addition, all proficiency testing is kept up-to-date. Although reagents and documentation are organized and well maintained throughout the year, I perform a walk-through of the laboratory before any inspection and review all documentation for errors."

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How to Answer: What is your experience with following procedure, preparing for, and being involved in a regulatory audit and/or inspections of any kind?

Advice and answer examples written specifically for a Clinical Research Associate job interview.

  • 2. What is your experience with following procedure, preparing for, and being involved in a regulatory audit and/or inspections of any kind?

      What You Need to Know

      As a Clinical Research Associate, you will likely encounter an audit or inspection of some kind, whether internal or external. The type of audit and/or inspection varies depending on the type of organization and the type of lab testing done at the facility. Your answer should reflect your experience and your awareness of expectations for the position you are interviewing for.

      Many companies and industries are subject to regulatory oversight and audits, and employees must be knowledgeable and capable in these areas. Additionally, having experience with audits and inspections can demonstrate attention to detail, compliance with regulations, and the ability to work effectively under pressure.

      Written by Krista Wenz on May 15th, 2023

      Answer Example

      "I have prepared for a Clinical Laboratory Improvement Amendments (CLIA) inspection by closely following all protocols while having good documentation practices. In addition, all proficiency testing is kept up-to-date. Although reagents and documentation are organized and well maintained throughout the year, I perform a walk-through of the laboratory before any inspection and review all documentation for errors."

      Written by Krista Wenz on May 15th, 2023