The post holder will work as part of a team of data management/study coordination staff providing comprehensive data management and trial coordination support to the department.
Responsibilities will include ensuring that clinical data required for CRF adopted trials are completed, validated and returned to study sponsors in an accurate and timely fashion, promoting high quality research, both within the Trust, nationally and Internationally.
The post holder will work as part of a team that provides the focal point for information requests and queries within the department. The post holder will ensure the clinical data collection, entry and transfer of information is of the highest standard and will be expected to be part of a team which develops the existing data storage systems and processes associated with them, as the needs of the service change.
The post is part of a team of data and study coordination staff in the CRF and as such the post holder will be expected to work as part of this team, providing cover for other members of the team when necessary and working together to pro actively improve data management within the department.