Jens-Olaf Vanggaard is Head of HighPoint’s Global R&D Practice based out of Zürich, Switzerland, and has more than ten years of experience providing advisory and implementation services regarding clinical development and regulatory affairs of the Life Sciences industry. Jens-Olaf has strong domain expertise within IDMP, regulatory information management (RIM), master data management (MDM), and data governance. These skills have been honed through extensive project work, participation in industry initiatives such as EMA; SPOR; and CDISC CTR2, and the development of IDMP tools and accelerators. Jens-Olaf has an MSc. in Computer Science and Business Administration from Copenhagen Business School.