Ulrike Fuchs has extensive experience in clinical operations and regulatory affairs within the pharmaceutical and biotechnology sectors. Currently serving as a Clinical Operations Manager at Valneva since February 2020, Ulrike previously held the position of Associate Clinical Operations Manager. Prior roles include Clinical Research Associate at IQVIA and EU Regulatory Affairs positions at Takeda and Shire, where Ulrike transitioned from a Regulatory Affairs Associate to a Product Specialist. Earlier career experiences include regulatory affairs internship at Baxalta and project assistance focused on quality assurance at the Research Institute for Applied Bioanalytics and Drug Development. Ulrike began a career in cancer research as a Melanoma Research Intern at the California Pacific Medical Center Research Institute. Educational qualifications include a Master of Science and Bachelor of Science in Medical and Pharmaceutical Biotechnology from IMC Krems University of Applied Sciences.
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