Sarah McLaughlin is an experienced clinical data standards expert currently serving as Associate Director of Study Data Standards Quality Management at Merck. They have developed and maintained data standards in the pharmaceutical industry, specializing in submission-ready datasets across various therapeutic areas. Previously, Sarah worked at institutions such as Biogen, Amgen, and Syneos Health, contributing to numerous clinical studies and leading data standards teams. They hold a BA in History from Boston College and an MPH in Epidemiology from The George Washington University.
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Boston, United States
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