Essential Skills for Clinical Research Associates/Monitors
Controlling the quality in clinical trials is essential. Monitoring of clinical trial data and investigational sites is therefore a prerequisite for all clinical trials and is also outlined in international guidelines for clinical research (ICH). This five-day course has been designed to prepare personnel new to the role and responsibilities of a Clinical Research Associate/Monitor. The course also incorporates some soft skills training appropriate for this role.
| Wann |
03.10.2011 um 09:00 bis 07.10.2011 um 17:00 |
|---|---|
| Wo | Vienna |
| Name | Christina Groiss |
| Kontakttelefon | 0043171340510 |
| Termin übernehmen |
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KEY TOPICS
- Site selection process
- Site preparation and initiation
- Monitoring responsibilities
- Essential documents
- Data management
- Study drug management
- Safety reporting
- Identifying and managing compliance and non-compliance; including audits and inspections
- Site closure
- Soft skills workshops (optimizing communication and time management and prioritization)
