Clinical Trial IT and Programming Manager
As Clinical Trials Programmer, my primary role is to assist in the development and maintenance of clinical trial databases and their associated interfaces and applications.
Study databases must be maintained to an extremely high level of security, validity and accountability to ensure that high quality data is available for analysis.
I also help to develop and maintain software and web applications that are used during the course of a study – such as a randomisation application and supporting web sites.
In the future the CTU are planning to increase the availability of Electronic Data Capture (on and off line) at study sites and GP offices via the development of web services and iPad apps
Support through Mobile Messaging and digital health Technology for Diabetes (SuMMiT-D) feasibility trial: strategies and data collection for monitoring of rapid recruitment in a primary care setting
Riga E. et al, (2019), TRIALS, 20