Karin de Haart is an experienced professional in the field of real-world evidence and regulatory safety, currently serving as Product Lead and Director at IQVIA since October 2014. In this role, Karin leads the strategy and development of Real World Evidence Regulatory & Safety offerings, focusing on Post-Authorization Safety Studies (PASS), particularly in pregnancy outcome studies and vaccine surveillance. Previous positions at IQVIA include Associate Director and Global Solutions Manager, where efforts were centered on clinical development and data-driven insights. Earlier career experiences include roles at Quintiles - Outcome and Outcome, emphasizing project management, coordination of international studies, and site management. Karin holds a Master of Science in Health Sciences from Vrije Universiteit Amsterdam and a Bachelor of Science in Health Sciences from Maastricht University.
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