When answering this question, focus on your direct experience with clinical trial monitoring. Highlight specific trials you have worked on, your role in those trials, and the outcomes. Discuss your familiarity with regulatory requirements and how you ensure compliance. Provide examples of challenges you faced and how you overcame them. For instance, you might say:
"In my previous role at XYZ Pharma, I monitored Phase III clinical trials for a new oncology drug. I was responsible for site selection, initiation, and close-out visits, ensuring all activities complied with FDA regulations. One challenge was ensuring timely data entry from multiple sites, which I addressed by implementing a more efficient communication protocol. This resulted in a 20% improvement in data entry timelines."
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