About me
Ruthie Davi is Senior Vice President, Statistics and Regulatory Science Innovation at Medidata, and has a background in pharmaceutical clinical trials with more than 20 years working at the FDA, most recently as a Deputy Division Director in the Office of Biostatistics in CDER. At Medidata Ruthie is part of a team using data science to create analytical tools to improve the efficiency and rigor of clinical trials. Ruthie’s recent work is focused on creation and analysis of synthetic or external controls, and she has numerous publications on this topic. Ruthie holds a Ph.D. in Biostatistics from George Washington University.
