Amanda Timm

Amanda Timm is a Senior Manager of Medical Writing at Quest Diagnostics, where they supervise the authorship of over 500 nonclinical protocols and reports and contribute to FDA, PMDA, IVDD, and IVDR submissions. Previously, they held roles such as Associate Director of Medical Writing at Invitae, where they established and expanded the writing team and developed essential tracking systems. Amanda earned a Ph.D. in Molecular, Cellular, and Developmental Biology from the University of California, Santa Barbara, where they also completed a Management Practice Certificate in the Technology Management Program. Their expertise includes precision oncology and compliance with Good Clinical Practice and Good Laboratory Practice.