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Mr. Vanggaard is the head of HighPoint’s global R&D practice based out of Zürich, Switzerland. Jens-Olaf has more than 10 years of experience providing advisory and implementation services within Clinical Development and Regulatory Affairs.
Jens-Olaf has strong domain expertise within IDMP, Regulatory Information Management (RIM), Electronic Trial Master File (eTMF), Clinical Trial Management Systems (CTMS) and Clinical Data Warehousing (CDW).
Jens-Olaf been deeply engaged in the topics of IDMP and end-to-end RIM for the last 3 years leading projects to assess the impact of and prepare for the implementation of IDMP for more than 5 clients.
Mr. Vanggaard has a MSc. in Computer Science and Business Administration from Copenhagen Business School.