Module Summary
Please find in this module all the documents and supporting materials required to successfully complete your immersion week at the Department of Clinical Research (DCR) Bern.
If you have any questions, please contact education.dcr@unibe.ch
Learning outcomes
At the end of this experience, participants will be able to:
- Analyze the roles and responsibilities of key stakeholders involved in clinical research, and differentiate how their contributions impact trial conduct and outcomes.
- Evaluate the functions of Departement of Clinical Research (DCR) within the Swiss clinical research landscape, and assess their contributions to study quality and efficiency.
- Critically assess current clinical research priorities in Switzerland, with a focus on professionalization, and interpret their implications for clinical trial practice.
- Apply principles of patient and public involvement (PPI) to design ethically and socially responsive clinical trial approaches.
- 5. Design and develop key elements of a clinical trial protocol (e.g., study design, endpoints, stakeholder integration) in collaboration with DCR support structures.
Learning objectives
- Analyze the roles and responsibilities of key stakeholders involved in clinical research, and differentiate how their contributions impact trial conduct and outcomes.
- Evaluate the functions of the Department of Clinical Research (DCR)) within the Swiss clinical research landscape, and assess their contributions to study quality and efficiency.
- Critically assess current clinical research priorities in Switzerland, with a focus on professionalization, and interpret their implications for clinical trial practice.
- Apply principles of patient and public involvement (PPI) to design ethically and socially responsive clinical trial approaches.
- 5. Design and develop key elements of a clinical trial protocol (e.g., study design, endpoints, stakeholder integration) in collaboration with DCR support structures.
