Speaker Profile

Ph.D., Vice President, R&D Clinical Sequencing Division, Thermo Fisher Scientific
Biography

In this role, Dr. Godsey is responsible for driving development of Thermo Fisher Scientific’s next generation of life science, transitional medicine and IVD products, including establishing a best in class companion Dx program as the centerpiece for CSDs Oncology Portfolio. Prior to that, he served as Senior Vice President of Product and Technology Development at Roche Tissue Diagnostics/Ventana Diagnostics, where he was responsible for leading the technology strategy, product development and on-market support. In this role, Dr. Godsey, built Ventana’s CDx program supporting Genentech, as well as external pharma partners such as Pfizer. Prior to Roche, Dr. Godsey led R&D Teams at Digene, Veridex, Gen-Probe and Dade-Behring. Dr. Godsey has had the privilege of launching a number of molecular Dx industry firsts, including the first FDA approved auto matched, molecular Dx asseys for blood screening, STD Screening and CTCs. Dr. Godsey also brings general management experience to any new challenge he takes on. He holds a Ph.D. in biology from St. John’s University.

Talk

How Can We Democratize And Globalize NGS For Companion Diagnostics?
TBA

Session Abstract – PMWC 2019 Silicon Valley

Session Synopsis: Companion diagnostics (CDx) tests provide information that is essential for the safe and effective use of a corresponding therapeutic products, such as a drug. Tumor profiling NGS tests may include CDx claims that are prescriptive for a specific therapeutic product, and are supported by analytical validity and a clinical study.

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