At the end of this training course you will have an understanding of common tasks required of a Clinical trial coordinator (CTC), how and when to perform those tasks.
1. Understand how to prepare for a monitoring visit, what to expect during a monitoring visit and how to work effectively with a monitor.
2. Apply principles of issue and CAPA Management to address quality issues identified at site.
3. Define source documentation and understand the difference and importance of source. documents and CRFs and identify when certified copies of source documents are required.
4. Understand the reasons behind timely data entry.
5. Awareness of different EDC requirements.
6. Understand and apply principles of IMP management at site.
7. Understand and apply the concepts of effective delegation.
8. Describe the typical tasks of a CTC at TGI.