The Master Science Programme (MSc) "Clinical Trials: Design and Conduct " aims to provide high-level knowledge for the in-depth understanding and development of skills for the design and conduction of Clinical Trials.

The curriculum comprises:

A) The general principles of Clinical Trials: phases, sample selection for each phase, principles of randomization and error avoidance

B) Research methodology: principles of statistical research and application to Clinical Studies, critique and assessment of results of published Clinical Trials and systematic reviews, design of Clinical Studies, systematic reviews and meta-analyses, analysis and publication of results

C) Good clinical practice and regulations of regulatory authorities: regulatory and ethical framework and participant involvement, organization and execution of Clinical Trials in accordance with European and Greek Legislation.

The above mentioned Msc leads to a Master of Science.

For the award of the MSc, the following are required:

a) The collection of the required credits (90 ECTS) according to the current Curriculum

b) Success in course exams

c) The successful completion of the Internship and

d) The successful presentation of the Master’s Thesis.