Suzanne Fleming

Suzanne Fleming has extensive experience in regulatory affairs and clinical research, having held various leadership positions at organizations such as FHI 360 and Family Health International. At FHI 360, Suzanne served as Acting Director of Clinical Regulatory and Compliance, overseeing clinical research and regulatory compliance, and previously managed regulatory strategy for international and US submissions. As a Senior Regulatory Affairs Manager at Family Health International, Suzanne guided regulatory strategies for numerous clinical trials across diverse global regions, supporting projects in areas including reproductive health and infectious diseases. Additionally, Suzanne has provided regulatory assessments at Biotest Pharmaceuticals and worked as a Senior Regulatory Affairs Associate at Cato Research. Suzanne holds a Bachelor of Science in Biology from the University of North Carolina at Pembroke.