Jennifer Khiem

Jennifer Khiem has a diverse work history in the biopharmaceutical industry. Jennifer is currently serving as the Director of Regulatory Affairs at Sutro Biopharma, Inc. since June 2021.

Prior to their current position, Jennifer worked at Amgen for almost a decade. During their time at Amgen, they held various roles, including Director of Global Regulatory Affairs from March 2016 to June 2021, and Clinical Research Study Manager from November 2012 to March 2016.

Before joining Amgen, Jennifer worked at PRA Health Sciences as a Senior Clinical Trial Specialist from December 2009 to November 2012. Jennifer also gained experience as a Project Coordinator at Assent Consulting from December 2008 to December 2009.

Jennifer started their career at Exelixis, where they held the positions of Clinical Supplies Specialist from March 2008 to December 2008, and Assistant Research Scientist from March 2007 to March 2008.

At the beginning of their career, Jennifer worked as a Junior Specialist at UCSF Medical Center from August 2005 to March 2007.

Jennifer Khiem holds a Bachelor of Science (BS) degree in Microbiology, Immunology, and Molecular Genetics from the University of California, Los Angeles. Additionally, they have obtained a Master's degree in Regulatory Sciences from the University of Southern California.