Meredith Mayo

Meredith Mayo has been with Ora, Inc. since April 1999, serving in various roles including Clinical Operations Manager and Senior Clinical Trial Associate, where responsibilities include ensuring adherence to study protocols and regulatory guidelines, developing essential study materials, and maintaining regulatory compliance. Prior to this, Meredith held positions at Bausch & Lomb as a Quality Assurance Associate and at Textron as a Regulatory Affairs Associate. Meredith's extensive experience encompasses project management support, site regulatory document oversight, and audit preparation. Educational background includes studies at Northern Essex Community College.