National Cancer Institute, Center for Cancer Research provides education and training materials for cancer researchers (e.g., research nurses). The Clinical Research Operations Online Self Learning presentation serial provides a basic overview of clinical research.
If you are new to clinical trials, you will find easier to learn below modules in the following order. Select the 1 slide per page for initial viewing and hyperlink capability. The 6 slides per page is an option for printing as needed.
- Clinical Trial Design: 1 slide per page or 6 slides per page
- Protocol Development: 1 slide per page or 6 slides per page
- Phase 0 Clinical Trials: 1 slide per page or 6 slides per page
- Informed Consent Process: 1 slide per page or 6 slides per page
- Roles and Responsibilities of the Research Team: 1 slide per page or 6 slides per page
- Roles and Responsibilities of the Sponsor: 1 slide per page or 6 slides per page
- Clinical Data Management: 1 slide per page or 6 slides per page
- Documentation in Clinical Research: 1 slide per page or 6 slides per page
- Documenting, Recording, and Reporting of Adverse Events and Unanticipated Problems: 1 slide per page or 6 slides per page
- Regulatory Binder: 1 slide per page or 6 slides per page
- RECIST: Applying the Rules (optional): 1 slide per page or 6 slides per page
- Monitoring and Auditing of Clinical Trials: 1 slide per page or 6 slides per page
Resource: Accrual Net
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