Data Management for Clinical Research

The general learning objective of this Master’s programme is to provide comprehensive training for the following duties:

1. managing clinical data, from collection to handling and processing through to final transfer to statistics centres;
2. ensuring that studies are carried out in accordance with clinical best practice guidelines set out in Good Clinical Practice;
3. guaranteeing the coordination of the various aspects of experimentation and serving as a point of contact for those involved in experiments (doctors, nurses, pharmacists, biostatisticians) and for local and external regulatory bodies (healthcare authorities, ethics committees, pharmaceutical companies, CROs, monitors, coordination centres, co-operatives etc.).