When answering this question, focus on your direct experience with clinical trials and the specific statistical methods you have used to analyze clinical trial data. Mention any relevant software or tools you are proficient in, such as SAS, R, or SPSS. Provide examples of past projects or studies you have worked on, highlighting your role and the outcomes of your analysis. Emphasize your understanding of regulatory requirements and guidelines, such as GCP (Good Clinical Practice) and ICH (International Council for Harmonisation) guidelines. For example:
"In my previous role at XYZ Pharma, I was responsible for analyzing data from Phase III clinical trials using SAS. I developed and validated statistical models to assess the efficacy and safety of the drug. My analysis contributed to the successful submission of the drug to the FDA, and it was eventually approved for market release. I am also well-versed in GCP and ICH guidelines, ensuring that all my analyses comply with regulatory standards."
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