uniQure
Natascha Schillemans is a seasoned professional in regulatory affairs with extensive experience spanning over two decades in the biotechnology and clinical research sectors. Currently serving as Sr. Manager RA at uniQure since May 2016, Natascha oversees Clinical Trial Applications, scientific advice meetings with authorities, and various regulatory activities including Orphan Drug Designation and Environmental Risk Assessments. Prior roles include Senior Regulatory Affairs Associate with Genzyme Europe BV, where responsibilities included the planning and submission of Marketing Authorization Applications, and positions at ICON Clinical Research, Merck Serono, and Erasmus MC, contributing to clinical trial applications and research nursing. Natascha holds two Bachelor's degrees in Middle Management from Avans Hogeschool Breda, obtained in 1999 and 2002.
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