Angela Whatley PhD
About Angela Whatley PhD
Angela Whatley, PhD, serves as the Senior Director of Regulatory Affairs at BridgeBio, where she has worked since 2021. She has extensive experience in regulatory affairs and scientific research, with a strong background in molecular biology and policy analysis.
Work at BridgeBio
Angela Whatley serves as the Senior Director of Regulatory Affairs at BridgeBio, a position she has held since 2021. In this role, she is responsible for overseeing regulatory strategies and ensuring compliance with relevant regulations for biological products. Her expertise in FDA Biologics Regulation supports the company's mission to advance innovative therapies.
Education and Expertise
Angela Whatley earned her PhD in Molecular Microbiology and Immunology from the University of Missouri-Columbia, where she studied from 2006 to 2012. She also holds a Bachelor of Science in Biology from Rockhurst University, completed from 2001 to 2005. Her educational background provides a strong foundation for her work in regulatory affairs and scientific research administration.
Background
Angela Whatley has a diverse professional background in regulatory affairs and scientific research. She began her career as an intern at the Wadsworth Center in 2003. She then worked as an Assistant Scientist at the Midwest Research Institute in 2005. From 2016 to 2021, she served as a Biologist at the FDA in Silver Spring, Maryland, where she gained significant experience in regulatory processes.
Previous Roles at U.S. Department of Veterans Affairs
Angela Whatley worked at the U.S. Department of Veterans Affairs in two capacities. She was a Presidential Management Fellow from 2012 to 2014 and later served as a Program Coordinator from 2014 to 2016. These roles allowed her to develop skills in policy analysis and program management, which are essential for navigating regulatory frameworks.
Analytical Skills and Scientific Management
Angela Whatley possesses strong analytical skills that enhance her capabilities in scientific research administration. Her background in molecular biology contributes to her effectiveness in managing scientific research pipelines. This expertise is critical in her current role, where she oversees regulatory affairs and ensures compliance with industry standards.