• Participation in the planning of the central data monitoring activities
  • Validation of study-specific data
  • Compilation of data reports & query management
  • Contact person for all project stakeholders
  • Participation in consultancy services and providing support for study sites and sponsors regarding regulatory questions and tasks
  • Participation in GCP-teaching courses for clinical research professionals
  • since 2018
    Clinical Trial Monitor, CTU Bern, University of Bern
  •  2017
    Central Data Monitor, CTU Bern, University of Bern
  • 2015
    Student Assistant, IPT University of Zurich/INSERM Paris
  • 2014-2015
    Master of Science in Human Biology, University of Zurich
  • 2009-2013
    Bachelor of Science in Biology, University of Zurich