GRAIL
Jolette Franco currently serves as the Sr. Director of Regulatory Affairs at GRAIL, Inc. since September 2021, overseeing FDA submissions and the maintenance of approved products. Previously, Jolette held the position of Sr. Director of Regulatory Affairs at Myriad Genetics from September 2010 to October 2021, where responsibilities included managing FDA regulatory compliance for two Class 3 PMA approved CDx LDT tests. Jolette has also progressed through various regulatory roles at Myriad Genetics, including Director, Manager, and Regulatory Compliance Coordinator, focusing on regulatory submissions to the FDA and other agencies. Earlier experience includes serving as Director of Operations at Talecris Plasma Resources and Center Manager at Octapharma. Jolette holds an MBA from the University of Utah - David Eccles School of Business and a CLS in Medical Technology from Weber State University.
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