Shionogi
Judy Tonkin is an experienced TMF Manager at Shionogi Inc. since June 2023, overseeing document control processes for GCP activities in compliance with regulatory requirements. Prior roles include Senior Associate Clinical Project Manager at SPARC, Regional Study Manager at InClin, and Senior Clinical Study Associate at Daiichi Sankyo, with responsibilities ranging from operational management of studies to regulatory support. Additional experience includes positions in regulatory affairs and project management at companies such as Genpact Pharmalink, IKARIA, Sanofi Pasteur, Novartis Pharmaceuticals, LifeCell Corporation, and Durata Therapeutics. Judy holds a BS in Psychology from SUNY New Paltz and has developed a strong background in compliance, documentation, and clinical study management throughout a diverse career in the pharmaceutical industry.
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Shionogi
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Shionogi Inc. is the U.S. subsidiary of Shionogi & Co., Ltd., a 140-year-old global pharmaceutical company with headquarters in Osaka, Japan. In the U.S., Shionogi Inc. leverages their science-based heritage to develop and commercialize pharmaceutical products to treat unmet medical needs in our core areas of infectious diseases and pain, as well as other areas of high medical need, including chronic liver disease.