Jennifer Chiu, Pharm D
About Jennifer Chiu, Pharm D
Jennifer Chiu, Pharm D, is the Director of Global Regulatory Affairs at BeiGene, with over 8 years of experience in global drug development focusing on oncology programs.
Current Role at BeiGene
Jennifer Chiu serves as the Director of Global Regulatory Affairs at BeiGene, a position she has held since March 2021. In this capacity, she is responsible for the oversight and implementation of regulatory strategies for oncology programs across multiple international regions, including the US, EU, and China. Her role involves coordinating with various departments to ensure compliance with regulatory requirements, facilitating communication with global health authorities, and contributing to the development and execution of regulatory plans that support the overall objectives of BeiGene's oncology initiatives.
Previous Experience at BeiGene
Before stepping into her current role, Jennifer Chiu was the Associate Director of Global Regulatory Affairs at BeiGene from 2019 to 2021. This role was based in the San Francisco Bay Area, where she focused on regulatory strategy and execution for both early and late-stage oncology programs. Her responsibilities included managing regulatory submissions, ensuring adherence to regulatory guidelines, and collaborating with cross-functional teams to drive program success. Her contributions in this capacity laid a solid foundation for her promotion to the Director role.
Career at Puma Biotechnology and Pfizer
Jennifer Chiu's career in regulatory affairs also includes significant roles at Puma Biotechnology, Inc. and Pfizer. At Puma Biotechnology, she worked as the Senior Manager of Global Regulatory Affairs from 2017 to 2018 in the Greater Los Angeles Area, where she was involved in regulatory strategies for oncology products. Prior to that, she served as Manager of Global Regulatory Affairs at Pfizer from 2016 to 2017 in the San Francisco Bay Area, focusing on regulatory requirements and submissions for global drug development programs.
Early Career and Education
Jennifer Chiu began her career as a Post Doctoral Fellow in Regulatory Affairs and Global Product Strategy at Genentech from 2013 to 2015, based in the San Francisco Bay Area. Prior to that, she gained experience at the FDA as a Pharmacy Intern in the Office of Prescription Drug Promotion in 2012. Her educational background includes a Doctorate in Pharmacy from The University of Texas at Austin, where she studied from 2009 to 2013. This combination of early career experience and advanced education laid the groundwork for her subsequent roles in regulatory affairs.
Expertise in Oncology Regulatory Affairs
With over 8 years of experience in global drug development, Jennifer Chiu specializes in clinical and nonclinical regulatory strategy and execution for oncology programs. Her expertise covers both early and late-stage developments, and she has a proven track record in navigating regulatory landscapes for key international regions such as the US, EU, and China. Her strategic insights and leadership capabilities have driven the success of multiple oncology programs, positioning her as a respected authority in the field of regulatory affairs.