Sample interview questions: Can you describe your experience in coordinating and facilitating participant consent or assent processes in clinical research studies involving minors or vulnerable populations?
Sample answer:
In my role as a Clinical Research Coordinator, I have extensive experience in coordinating and facilitating participant consent or assent processes in clinical research studies involving minors or vulnerable populations. This experience has allowed me to develop a deep understanding of the ethical considerations, legal requirements, and best practices involved in obtaining informed consent or assent from these populations.
When working with minors, I ensure that the consent process is age-appropriate and tailored to their developmental level. I take the time to explain the study in a clear and understandable manner, using language that is appropriate for their age and comprehension. I also prioritize establishing a comfortable and trusting relationship with both the minor and their parent or legal guardian, as their involvement is crucial in the consent process.
To facilitate the consent process, I provide all relevant information about the study, including its purpose, procedures, potential risks and benefits, and any alternatives to participation. I encourage questions and address any concerns or uncertainties that may arise, ensuring that the minor and their parent or legal guardian fully understand the study before making a decision. I also emphasize that participation is voluntary and that they have the right to withdraw at any time without consequences.
For vulnerable populations, such as individuals with cognitive impairments or mental health conditions, I approach the consent process with additional sensitivity and adaptability. I take into account their unique needs, abilities, and potential challenges in understanding the study information. I may utilize visual aids… Read full answer
Source: https://hireabo.com/job/7_0_31/Clinical%20Research%20Coordinator