Sarah Kurihara is a Sr. Data Scientist supporting the Global Clinical Trial Operations (GCTO) team at Merck. Currently, she is using Real World Data (RWD) to inform strategic planning of clinical trial studies. Prior to joining Merck, Sarah spent four years in the medical device industry as a Design Quality Engineer and Data Scientist with Ethicon, a Johnson & Johnson MedTech company. She holds a BS in Biology (University of Oregon), an MEng in Biomedical Engineering (Boston University), and an MS in Operations Research (Columbia University).

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