Mai-Ly Wilcox

Senior Director Regulatory and Clinical Affairs at Venclose

Mai-Ly Wilcox has worked in the regulatory and clinical affairs field since 2001. Mai-Ly began their career as a QC/QA Chemist at ALZA (Johnson & Johnson) in 2001. In 2004, they moved to Abbott Vascular Inc (formerly Guidant Corporation) as a Stability QE. In 2007, they joined VNUS Medical Technologies as a Senior Regulatory Affairs Associate and Senior QE. In 2011, they became a Senior Regulatory Affairs/Quality Assurance Engineer at Curexo Technology Corporation. In 2012, they moved to Miramar Labs, Inc. as a RA Project Manager. In 2016, they returned to Venclose as a RA/QA Manager. In 2017, they joined Silk Road Medical, Inc. as a Principal Regulatory Specialist and Scanadu as a RA Manager. Finally, in 2019, they returned to Venclose as Senior Director Regulatory and Clinical Affairs and Director, Quality, Clinical and Regulatory Affairs.

Mai-Ly Wilcox obtained a Bachelor of Science (B.S.) in Chemistry from the University of California, Davis between 1996 and 2000.

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Timeline

  • Senior Director Regulatory and Clinical Affairs

    May, 2021 - present

  • Director, Quality, Clinical and Regulatory Affairs

    August, 2019

  • RA/QA Manager

    January, 2016

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