In the past two decades, the number of Clinical Trials conducted in Switzerland and worldwide has virtually exploded.

This tremendous increase went hand in hand with the development of codes, guidelines and regulations aimed at protecting human research subjects.

Standardization and strengthening of clinical research regulations have led to the development of a rapidly growing economic sector in which Clinical Research Associates (CRA), Clinical Research Scientists (CRS), Data Managers (DM), Clinical Research Coordinators (CRC), Clinical Trial Managers (CTM) and regulatory affairs specialists are key players.

The Diploma of Advanced Studies in Management of Clinical Trials– Good Clinical Practice Implementation and Quality Processes provides a theoretical and practical understanding of how Good Clinical Practice (GCP) principles are shaping each step of a Clinical Trial, including study design, trial management and conduct as well as data management and analysis.

The course draws on the expertise of professionals from academic institutions, pharmaceutical companies and Contract Research Organizations (CRO) and provides a unique opportunity to conduct a 3 to 4 months vocational training in clinical research. Further information may be found at:

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