Sample interview questions: Can you explain your familiarity with research compliance and regulatory protocols in medical research?
Sample answer:
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Experiences with Institutional Review Boards (IRBs): I have extensive experience working with IRBs to obtain ethical approval for research projects, ensuring that they adhere to ethical guidelines and protect the rights and welfare of human research participants.
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Understanding of GCP (Good Clinical Practice): I am highly familiar with GCP guidelines and regulations, including the principles of informed consent, data management, and adverse event reporting. I have worked to ensure compliance with GCP standards in various research studies.
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Knowledge of HIPAA (Health Insurance Portability and Accountability Act): I understand the requirements of HIPAA and have implemented measures to protect the privacy and confidentiality of research participants’ health information. I have also ensured that research protocols include appropriate data security measures.
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Compliance with FDA (Food and Drug Administration) Regulations: I am familiar with FDA regulations related to medical research, including the requirements for clinical trials and investigational new drugs. I have assisted in the preparat… Read full answer
Source: https://hireabo.com/job/2_3_28/Research%20Assistant