Sample interview questions: Can you explain the process you follow for obtaining informed consent from study participants?
Sample answer:
The process of obtaining informed consent from study participants is a crucial aspect of ethical clinical research. As a Clinical Research Coordinator, my primary responsibility is to ensure that participants fully understand the purpose, procedures, risks, and benefits of the study before voluntarily agreeing to participate. Here is a detailed explanation of the process I follow for obtaining informed consent:
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Initial contact and screening: Once potential participants are identified, I would provide them with an overview of the study and assess their eligibility. This initial contact helps establish rapport and allows me to answer any preliminary questions they may have.
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Detailed explanation: During an in-person meeting, I would provide participants with a detailed explanation of the study, including its purpose, procedures, and expected duration. I would also explain any potential risks, benefits, and alternatives to participation. It is important to present this information in a clear and understandable manner, avoiding any technical jargon.
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Q&A session: After presenting the study details, I would encourage participants to ask questions to clarify any doubts or concerns they may have. This session aims to ensure their comprehension of the study requirements and allows me to address any misconceptions or fears they may have.
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Written consent form: Once participants have had an opportunity to ask questions and fully understand the study, I would provide them with a written consent form. This document includes all the relevant study information discussed previously. Part… Read full answer
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