Sample interview questions: Have you worked with research monitors or auditors to ensure compliance with study protocols and regulatory requirements?
Sample answer:
- Collaborated closely with research monitors and auditors to ensure compliance with study protocols and regulatory requirements in multiple clinical research studies.
- Actively participated in pre-study initiation visits, monitoring visits, and close-out visits, working diligently to resolve any discrepancies or issues promptly.
- Proficiently reviewed and assessed study documentation, including informed consent forms, adverse event reports, and patient medical records, to ensure completeness, accuracy, and adherence to protocol guidelines.
- Conducted comprehensive data quality checks and audits to identify and rectify any data discrepancies or inconsistencies, ensuring the integrity and reliability of research data.
- Collaborated effectively with investigators, study coordinators, and other research personnel to address any protocol deviations or regulatory concerns, providing guidance a… Read full answer
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