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For 1 week, course participants
- observe consultations for various clinical trials, including obtaining informed consent and administration of trial procedures and therapies
- interact with research teams; patients and their families; and PPI contributors to understand why clinical research is important
- understand the different roles of people involved in clinical research
- demonstrate value-based knowledge of PPI when conducting clinical trials
- explain clinical research priorities in Switzerland related to professionalization
- describe how CTUs and CIUs contribute to clinical research in Switzerland
- develop different clinical research and clinical trial design elements with support from DCR Bern
Please note that the schedule depends on team availability, ongoing projects, and confidentiality requirements, so some activities may not be open to observation. |