Anna Riese is currently the Clinical Affairs and Regulatory Affairs Manager at VYSYO GmbH, with expertise in Clinical Research, Medical Writing, QMS, Risk Management, Clinical Evaluation, and Clinical Investigation. Prior to this, Anna worked as a Klinischer Monitor at DZNE - German Center for Neurodegenerative Diseases, where Anna focused on On-Site Monitoring, Data Cleaning and Management, and eCRF. Additionally, Anna served as a Wissenschaftlicher Mitarbeiter mit akademischem Abschluss at Institut für Empirische Gesundheitsökonomie, specializing in Monitoring, Health Economics, Project Management Clinical Trials, and Systematic Reviews.
May, 2022 - present
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