Chiara Lazzarin

Chiara Lazzarin is a Senior Regulatory Affairs Specialist with extensive experience in clinical research and regulatory submissions. They have worked with notable organizations, including PPD and Novartis GenMed, where they developed strategies for regulatory compliance and led project-specific processes. Chiara holds a Master of Science (MSc) in Experimental Thesis focused on HIV+ patients from Università degli Studi di Milano and has expertise in databases, EU CTR submissions, and good clinical practice guidelines. Prior roles include Clinical Research Associate and Country Approval Specialist, demonstrating a strong foundation in medical research and regulatory affairs.