Priavoid’s management team has comprehensive experience in scientific research, preclinical- and clinical development, quality management, regulatory compliance, and business development.
Dr. Sabine Willbold
Dr. Sabine Willbold studied Chemistry at the University of Bayreuth (Germany) and received her PhD in anorganic chemistry. She gained industrial experience in a couple of companies and went back to academic research in the field of peptide synthesis at the University of Jena (Germany). In 2002, she joined the Jülich Research Centre at the Institute of Analytics (ZEA-3), where she became deputy director in 2011. She is expert in a broad band of chemical analytics and collected experience as CEO since 2017. She has recently joined Priavoid to serve as Managing Director.
Dr. Antje Willuweit
Managing Director and Director of Preclinical Research
Dr. Antje Willuweit studied Biology at the Technical University of Darmstadt (Germany) and received her PhD from the Max-Planck-Institute in Bad Nauheim (Germany). She gained 9 years of industrial experience in the following Biotech companies: Artemis Pharmaceuticals GmbH, Evotec Neurosciences AG, Evotec AG. In 2011 she joined the Jülich Research Centre at the Institute of Neuroscience and Medicine (INM-4), where she established her own research group. In total, she has got 20 years of experience with animal models in preclinical research, including at least 13 years in the field of preclinical drug testing against Alzheimer´s disease and other neurodegenerative diseases. She co-founded Priavoid in 2017 and is since then Director of Preclinical Research. Recently, she became also Managing Director in parallel.
Dr. Dagmar Jürgens
Director Clinical Research
Dr. Dagmar Jürgens studied Agricultural Sciences at University of Göttingen (Germany) and subsequently earned her PhD at the University of Gießen. She gained experience at national and international levels since 1990, after founding and leading a small and medium-sized biotech enterprise for more than 15 years. In 2006 she changed her focus to Clinical Research and Drug Development. She furthered her experience in Phase II and III Clinical Trials, whilst working at the German Competent Authority (BfArM) and with international Contract Research Organizations. She has been working at the Jülich Research Center since 2011, first at the Technology Transfer Department, and then at the Institute of Complex Systems (ICS-6), where she is the Project Manager for Preclinical and Clinical Research. She co-founded Priavoid in 2017 and is since then Director of Clinical Development.
Dr. Knut Adermann
Dr. Knut Adermann has more than 20 years experience in peptide therapeutics discovery, translational medicine and clinical development, with a focus on the chemistry, manufacturing and control of novel, peptide active pharmacological ingredients. He holds a PhD in organic chemistry and has co-founded several biotech start-ups, pursuing indications in the fields of antivirals and antibacterials. He was involved in the successful sourcing of seed and round A financing for various start-up companies and has served as managing and scientific director of these ventures. As a consultant in peptide development, he has also supported various preclinical and clinical programs in cardiology, hematology and metabolic diseases. He is an author of more than 90 publications and is a co-inventor of numerous internationally filed patents and patent applications. He co-founded Priavoid in 2017 and is since then Director of CMC.
Dr. Gunther Kauselmann
Director of Quality Management and Regulatory Compliance
Dr. Gunther Kauselmann studied Biology at the University of Hamburg and completed his PhD at the Center for Molecular Neuroscience Hamburg (ZMNH). In 1998 he joined the startup company Artemis Pharmaceuticals GmbH in Cologne, which was renamed Taconic Biosciences GmbH after being acquired by Taconic Biosciences Inc. in 2009. At Taconic Dr. Kauselmann held several management positions in scientific operations, quality management and regulatory compliance with increasing responsibility, before being appointed as Vice President of Operations to oversee the production process at the Cologne site. During his professional career he also graduated in Drug Regulatory Affairs and obtained his Master´s Certificate from the University of Bonn. He co-founded Priavoid in 2017 and is since then Director of QM and Regulatory Compliance.
Head of Study Coordination (designated staff member)
Stefanie Simons has completed an apprenticeship to assistant in a law office and more than 10 years of professional experience as senior project coordinator at Global Research Services and clinical trial assistant at UCB. She obtained comprehensive knowledge in conducting international Phase I – III studies as well as on non-interventional studies with a focus of Alzheimer´s, Parkinson, rheumatoid arthritis and pediatrics.