This includes clarifying and operationalising the primary and secondary objectives of clinical trials, the implications of design choices for implementation of a trial, trial governance, approvals (including Regulatory and ethics committee), and data collection and recruitment methods. The module will also explore quality assurance and control, and investigate both data processing and data management issues.
15 [150 hours]
Unseen written examination (2hr 15). If you fail the module, you are allowed one further attempt at the examination.
For full information regarding this module please see the module specification.