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Willette Jones Whitmore is a Certified Clinical Research Professional with over 20 years of diverse biotech industry experience in various phases of global clinical trials management and quality assurance (QA) for regulated medical devices, pharmaceuticals, and biologics. She has spent more than 12 years with CROs, focusing on compliance with global health authority regulations and ICH GCP guidelines. She is a transformational and innovative Leader with proven successes in developing global quality and clinical/operational teams, strategies, and other specialized services within QA. She has also authored various controlled documents, user manuals, course platforms, and training curricula.