ÂÜÀòÂÒÂ×

Heike S. possesses extensive experience in regulatory affairs, having served as the Regulatory Affairs Lead at Verily and held multiple director-level positions at Foundation Medicine, including Director of Regulatory Affairs for R&D and Technology, as well as Director of RA SW/Data Products. Prior to these roles, Heike S. contributed as a Subject Matter Expert and Principal Investigator at the FDA, specializing in next-generation sequencing. Additionally, Heike S. gained valuable research experience as a Postdoctoral Associate at the University of Florida Genetics Institute.