Clinical Trial Management and Statistics

Module Objectives

This module covers the practical management of the development of a medicine from Phase I to IV using research techniques to optimise efficiency in the development process.  It also teaches students how to critically review and evaluate statistical data and to leverage and use the information. 

Intended Module Learning Outcomes

Participate in most tasks needed to successfully conduct a clinical trial

Evaluate the suitability of different research methodologies for different types of clinical trials

Implement and manage suitable quality systems

Prepare and participate in audits and inspections.