Clinical Research Training for Senior CRAs 2014 is a course that covers topics such as:
- Refreshing and update of the current European legislation of clinical research
- Importance of international research – the role of the ICH process
- The informed consent: verification of the process
- Monitoring plan development
- Upgrading monitoring tasks: prioritizing tasks, better monitoring reporting, efficient tracking, dealing with non-compliances
- Improving recruitment of investigators and of study subjects
- Expedited safety reporting
- Quality systems and audits
Clinical Research Training for Senior CRAs 2014 is intended for:
- Experienced people working in clinical data processing
- Clinical Research Associates (CRAs) with min 2 years of experience
- Regulatory affairs
- Biostatistics