Description

These 12 online educational modules provide an introductory but comprehensive overview of the clinical research process for staff who are new to the clinical research arena.

Details

Details:

The following modules are included:

1. Clinical Trial Design
2. Protocol Development
3. Phase 0 Clinical Trials
4. Informed Consent Process
5. Roles and Responsibilities of the Research Team
6. Roles and Responsibilities of the Sponsor
7. Clinical Data Management
8. Documentation in Clinical Research
9. Documenting, Recording, and Reporting of Adverse Events and Unanticipated Problems
10. Regulatory Binder
11. RECIST: Applying the Rules (Optional)
12. Monitoring and Auditing of Clinical Trials