Pamela M.

Pamela M. is an experienced regulatory affairs professional with a career spanning over a decade in the life sciences industry. Since September 2013, Pamela M. has held various positions at KLS Martin Group, including Regulatory Affairs Project Manager, Regulatory Affairs Supervisor, and Regulatory Affairs Specialist. Prior experience includes a role as a Master Thesis Student at Gilead Sciences, where Pamela M. focused on enhancing clinical development for a respiratory drug through various regulatory filings and fulfilling FDA reporting requirements. In addition, Pamela M. worked as a Regulatory Affairs Consultant at Hammond Clinical Trial Consulting, developing strategies for innovative combination products, and served as a Research Assistant at Penn Medicine, contributing to post-market surveillance studies. Pamela M. holds a Master of Science in Biomedical Regulatory Affairs from the University of Washington, as well as Bachelor's degrees in International Livestock Production and Animal and Food Sciences.