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Liz Nulton-Bodiford, MS, has extensive experience in the pharmaceutical industry, beginning as a Document Processing Administrator at Burroughs Wellcome and advancing to various key roles at GSK, including Compliance Director for US Safety and Manager of Regulatory Quality Assurance. Notable contributions include serving on the CDASH team as a core member representing GSK, creating data collection standards, and leading the implementation of the Regulatory Affairs Quality Assurance Program globally. In addition to industry roles, Liz has been an Adjunct Professor at Campbell University, teaching Pharmaceutical Compliance & Quality Assurance in the Clinical Research program. Liz holds a Bachelor's degree from Emory and Henry College and a Master's degree from Campbell University.