Sheffield Teaching Hospitals NHS Foundation Trust
Job Summary
This vacancy is an exciting opportunity to support the delivery of research activity across the Renal and Vascular Academic Directorates within the South Yorkshire Regional Services (SYRS) care group. This role involves supporting the work of the Research Theme Leads, working closely with investigators, their clinical teams, and providing administrative and clinical support to the Renal and Vascular Directorate research teams.
The post holder will be responsible for supporting the Renal and Vascular Directorate Research Coordinator and the Principal Investigators to assist in increasing the research productivity, complete data entry and actively screen lists to increase the inclusion of potential participants into trials. The post holder will interact with patients to obtain clinical samples and perform clinical measurements (e.g. blood pressure, ECGs). The role will involve working closely with research and clinical teams to increase patient recruitment into clinical trials.
The post holder will also be required to maintain holistic support for all clinical trial participants, thus facilitating a high quality research service.The post holder will be expected to interact with patients and their families in relation to the requirements of the clinical trials and be able to work without supervision in some areas.
Main duties of the job
The post holder will assist in supporting a portfolio of clinical trials, from study set up to archiving, in accordance with clinical trial protocols,laboratory manuals and all relevant regulatory standards.
The role will involve collecting, recording and maintaining research data records, entering activity data and extracting information from databases, providing clinical and general administrative support to the research teams including performing clinical tests and investigations, processing and shipping samples and assisting with screening and recruitment processes. Clinical tasks will include, but not limited to, taking biological samples (blood, urine etc.), taking blood pressure and anthropomorphic assessments.
In addition, the post holder will have the responsibility of maintaining all clinical trial documentation according to regulatory, governance and Good Clinical Practice (GCP) requirements.
The post holder will be expected to undertake study-specific training for each trial.
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