For further information on this role, please see the attached detailed Job Description and Person Specification: Undertake data checking and generation of summary reports for trial data entered by research sites in line with the protocol, data monitoring plan, monitoring plan and requirements of oversight committees. Assist with the setting up of the trial master file (TMF) and with subsequent maintenance of the file. To liaise with trial managers and Good Clinical Practice (GCP) team regarding updates to the TMF as required. Assist with the preparation of investigator site files (ISF) and ensure site teams are aware of their responsibilities for the maintenance of the ISF at their site, as required. Liaise with staff at research sites to provide information and documentation and support the set-up, implementation of amendments and running of the trial at each site as required.