Jean Smart is a Regulatory Affairs and Quality Officer with over 30 years of experience in clinical trials and research regulation. She has contributed to numerous global regulatory initiatives and is actively engaged on national and international committees, project teams, and advisory boards.

Her academic background and professional focus center on global health and international development, particularly in research policy and governance. Jean is passionate about advancing research program development, building clinical trial capacity, and fostering research culture in emerging and under-resourced regions.