• Understand and use in a relevant context the different Clinical Trial designs and methodologies
  • Be familiar with drug development and marketing authorization processes
  • Gain knowledge of GCP and of clinical research regulations in Switzerland, Europe and the United States
  • Become skilled at developing Case Report Form (CRF)
  • Coordinate the development of clinical trial protocols
  • Master effective project planning and management
  • Know how to manage applications for Ethics Committee (EC) and Regulatory Authority (RA)
  • Understand and implement Quality Systems used in Clinical Trials
  • Understand the issues related to research subject protection