Tabitha Santoso

Tabitha Santoso is an accomplished professional in regulatory affairs with extensive experience in the pharmaceutical industry. Since March 2017, Tabitha has held multiple roles at BioMarin Pharmaceutical Inc., currently serving as Associate Director of Regulatory Affairs Clinical, and previously as Senior Manager in both Clinical and Chemistry Manufacturing Control (CMC) regulatory affairs. Tabitha's earlier career includes a position as Regulatory Associate IV at BioMarin (2016-2017), a Regulatory Affairs Senior Associate at Gilead Sciences (2014-2016), and contributing to regulatory submissions at BioMarin from 2006 to 2013. Additional experience includes quality control analysis roles at Vaxgen, Inc. and Anosys, alongside an administrative assistant position in regulatory affairs at Depomed, Inc. Tabitha holds a Bachelor of Science in Biological Sciences with a focus on Microbiology from the University of California, Davis.