After finishing my PhD in Medical Sciences, I have worked as a research scientist for several years. In those years I have managed several preclinical research projects involving neurological diseases and gained experience on process analysis and optimization. During my career in Regulatory Affairs, I have been involved in different projects, ranging from preclinical development to worldwide post-approval CMC changes for small molecules and biotech products. I speak and write in Dutch and English fluently. What I appreciate about Starodub is that my colleagues have different backgrounds and specialties, giving me the opportunity to work in a stimulating environment.