How do you ensure that the rights and welfare of study participants are protected at all times?

Sample interview questions: How do you ensure that the rights and welfare of study participants are protected at all times?

Sample answer:

As a Clinical Research Coordinator in the field of psychology, it is my utmost responsibility to ensure the protection of the rights and welfare of study participants at all times. To achieve this, I implement several measures:

  1. Informed Consent Process: I prioritize obtaining informed consent from all study participants. This involves providing them with detailed information about the study, including its purpose, procedures, potential risks and benefits, confidentiality measures, and their rights as participants. I ensure that participants have sufficient time to ask questions and make an independent decision about their participation.

  2. Ethical Review: I adhere to the ethical guidelines set forth by regulatory bodies such as the Institutional Review Board (IRB) or Ethics Committee. Before conducting any research, I submit a detailed protocol that outlines the study design, participant recruitment methods, and data collection procedures. This protocol is thoroughly reviewed to ensure that participants’ rights and welfare are protected.

  3. Confidentiality and Anonymity: I prioritize participant confidentiality by strictly adhering to privacy regulations. I take necessary measures to protect participants’ personal information, such as using participant codes instead of real names and storing data in secure, password-protected systems. I also ensure that only authorized personnel have access to the data.

  4. Risk Assessment and Minimization: I conduct a comprehensive risk assessment before starting any study. This helps me identify potential risks associ… Read full answer

    Source: https://hireabo.com/job/7_0_31/Clinical%20Research%20Coordinator

Leave a Reply

Your email address will not be published. Required fields are marked *