Heide Messner is a Clinical Trial Regulatory Manager and Regulatory Advisor with extensive experience in regulatory affairs. Currently at IQVIA since 2013, Heide leads regulatory consultancy efforts, ensuring compliance and high-quality standards in clinical trials. Previously, they held roles at Alcon Pharma GmbH and PAREXEL Nederland B.V., where they managed worldwide clinical trial regulations and mentored colleagues. Heide earned a Master of Science in Biology from Universität Konstanz.
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