Davy Chiodin
About Davy Chiodin
Davy Chiodin serves as the Chief Development Officer at Day One Biopharmaceuticals, bringing nearly 20 years of experience in the pharmaceutical industry, particularly in regulatory affairs and oncology development. He has held senior roles at notable companies such as Genentech and AstraZeneca, and has an extensive academic background in pharmacy and pharmacoeconomics.
Current Role at Day One Biopharmaceuticals
Davy Chiodin serves as the Chief Development Officer at Day One Biopharmaceuticals since 2021. In this role, he oversees a diverse range of functions, including Regulatory Science and Quality Assurance. He is involved in program management and product leadership, contributing to the company's strategic initiatives in drug development.
Previous Experience at Genentech
Chiodin has extensive experience at Genentech, where he held multiple senior roles. He worked as a Senior Regulatory Affairs Manager from 2009 to 2010 in Basel, Switzerland, and later as a Senior Program Director for Regulatory Affairs from 2014 to 2016 in South San Francisco. His tenure at Genentech spanned over 10 years, during which he assumed roles of increased responsibility in the Regulatory function.
Education and Expertise
Davy Chiodin holds a PharmD from the University of Grenoble, France. He has also earned two Master's degrees in Regulatory Affairs and Pharmacoeconomics from the Université René Descartes - Paris V and the University of Lille 1 Sciences and Technology. His educational background provides a strong foundation in pharmacoeconomics and regulatory affairs, which supports his professional expertise.
Experience in Oncology Development
Chiodin has nearly 20 years of experience in the pharmaceutical industry, with a significant focus on oncology development. He has 15 years of dedicated experience in this area, including two years fully dedicated to the pediatric oncology portfolio at Roche/Genentech. His experience positions him as a knowledgeable leader in oncology-related regulatory affairs.
Career Background at AstraZeneca and Acerta
Before his roles at Genentech, Davy Chiodin worked at AstraZeneca AB as an EU/Global Regulatory Affairs Manager from 2003 to 2005 in Sweden. He also worked at Acerta, a member of the AstraZeneca group, where he led Regulatory Science and Quality Assurance functions. His career reflects a strong commitment to regulatory affairs across multiple leading pharmaceutical companies.