This service is designed to strengthen the skills of the persons involved in the clinical trials by providing training on the following :
Expertise, by offering introduction or advanced courses on clinical data management and various statistical analysis techniques. Additionally offering the possibility to apply this knowledge in view to the initial writing and conception of the clinical trial protocol.
Improve communications by providing notions on statistics and data management to physicians, monitors, investigators. Provide related articles, reading materials and presentations, including the results of clinical trials thus enabling the different professionals involved in the clinical research to gain mutual understanding of the expectations and obligations by having a better knowledge of each others role in the clinical trial.
- To improve understanding of statistics and clinical data management in order to contribute to better job performance (monitors, physicians, investigators, etc.).
- Prepare, validate, store and manage clinical data (methods, reasons and tools).
- Analysis of continuous or qualitative data, time-to-event data and time-depending data.
- Data exploration (principal components analysis, simple or multiple correspondance analysis, classification, ...).
- Statistical methods for the design of clinical trials.