Milica Ćuk is a Senior Regulatory Affairs Manager at PPD, where they oversee clinical trials across Europe, MENA, North America, and Asia-Pacific. Previously, Milica held various roles at INC Research and Syneos Health, including Senior Start-Up Project Delivery Manager and Regulatory Site Activation Manager, where they managed site activation processes and ensured compliance with regulations. Milica's earlier experience includes being a Senior Regulatory Affairs Associate at Accelsiors CRO and a Marketing Associate at Hemofarm AD. Milica earned a Master of Science in Pharmacy with a focus on Medical Biochemistry and completed postgraduate studies in Pharmacoeconomics and Pharmaceutical Legislation at the University of Belgrade.
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