Suzanne Fleming

Suzanne Fleming has extensive experience in regulatory affairs and clinical research, currently serving as Acting Director of Clinical Regulatory and Compliance at FHI 360 since April 2012. In this role, Suzanne provides oversight for clinical research and regulatory compliance, developing policies and procedures to meet management and government compliance objectives. Prior positions include Manager of Regulatory Affairs, where regulatory strategy for international and US submissions was a focus, and research associate roles emphasizing quality assurance and regulatory compliance across various countries and therapeutic areas. Suzanne also held managerial and consulting roles at Family Health International and Biotest Pharmaceuticals, managing regulatory strategies for clinical trials and ensuring compliance with international laws and guidelines. Academic credentials include a Bachelor of Science in Biology from the University of North Carolina at Pembroke.