Clinical Research Fellow (Haematology)

Supporting the coordination, management and delivery of clinical trials and studies according to protocols. Supporting the Principal Investigator and/or the Departmental Research Lead in submitting applications for NHS, Regulatory, Ethics and Governance permissions to conduct Clinical Trials within the Trust. Identifying, screening, and assessing the suitability of local patients to take part in research, according to specified inclusion/exclusion criteria. Ensuring trial specific investigations and sampling are undertaken as per the Protocol to establish eligibility and to ensure safe entry into trials. Providing specialist information to patients about taking part in Clinical Trials, including the risks and benefits of participation in specific protocols. Initiating and facilitating the process of gaining their informed consent. Acting as primary contact for participants and to be a source of information for these patients and their relatives and for the local Clinical teams, with respect to trial activities. Liaising with other clinical departments, support departments and external organisations to ensure the successful delivery of trials. Maintaining accurate documentation in an auditable format, and accurately record data as required by each Trial. Identifying barriers to recruitment and performance, communicating these to the wider team, and help facilitate their resolution. Working to Standard Operating Procedures (SOPS) for research activity and provide ongoing review and development of these SOPS. Ensuring all activities undertaken meet the standards set out in the Principles of GoodClinical Practice (ICH-GCP, 1996) and National Research Governance Framework for Health & Social Care (DH, 2005). Enforce all applicable standards (e.g., Medicines for Human Use (Clinical Trials) Regulations 2004) for research. Undertaking research projects in Haematology. The post holder will be encouraged to register for an MD thesis or similar and present their findings at national meetings as well as publishing in peer reviewed journals. Assisting with running current multi-centre clinical research trials recruitment, consenting, performing procedures as per protocol. On completion of the trial data analysis, publishing of results and writing papers. Write grant applications for future studies, as identified. Actively participate in the research team meetings, including current research fellows, research nurses and department consultants