Bethany Goodrich, Ms
About Bethany Goodrich, Ms
Bethany Goodrich is an Associate Director of Regulatory Advertising & Promotion at Aimmune Therapeutics, where she has worked since 2019. She has extensive experience in regulatory affairs, having held various positions at Rigel and FibroGen, and holds a Master of Science in Regulatory Affairs from San Diego State University.
Work at Aimmune Therapeutics
Bethany Goodrich currently serves as the Associate Director of Regulatory Advertising & Promotion at Aimmune Therapeutics. She has been in this role since 2019, contributing to the regulatory landscape of advertising and promotional materials. Prior to her current position, she worked at Aimmune Therapeutics as a Senior Manager in Regulatory Affairs from 2016 to 2018 and as a Senior Manager in Regulatory Advertising & Promotion from 2018 to 2019. Her experience at Aimmune Therapeutics spans over four years, during which she coordinated the Promotional Review Committee and acted as the regulatory reviewer for advertising and promotional materials.
Previous Experience at Rigel
Bethany Goodrich has extensive experience at Rigel, where she held multiple positions over several years. She worked as a Senior Research Associate II from 2007 to 2011, and later as a Senior Regulatory Affairs Associate from 2011 to 2013. Additionally, she served as a Clinical Project Coordinator for six months in 2009 and worked as a Consultant from 2003 to 2007. Her early role at Rigel included serving as an Animal Care Specialist/Vivarium Coordinator from 2001 to 2002. This diverse experience provided her with a solid foundation in regulatory affairs and clinical research.
Education and Expertise
Bethany Goodrich holds a Master of Science in Regulatory Affairs from San Diego State University, which she completed between 2010 and 2012. She also earned a certificate in Clinical Research Conduct and Management from the University of California, Berkeley, from 2008 to 2009. Earlier, she obtained a Bachelor of Science in Animal Science from California Polytechnic State University-San Luis Obispo, completing her degree in 2001. Her educational background supports her expertise in regulatory affairs and clinical research management.
Achievements in Regulatory Affairs
Throughout her career, Bethany Goodrich has successfully managed regulatory submission timelines for products with significant safety considerations, including those with boxed warnings and Risk Evaluation and Mitigation Strategies (REMS) programs. She has also owned the Promotional Review Committee electronic Document Management System (PRC eDMS), overseeing its management and implementation. Her roles have involved critical responsibilities in ensuring compliance and facilitating effective communication within regulatory frameworks.