Clinical Research Nurse/Practitioner

at  Norfolk and Norwich University Hospital

To work according to ICH Good Clinical Practice (GCP) guidelines and research governance standards for clinical trials and current Standard Operating Procedures (SOPs) To demonstrate in-depth knowledge of trial protocols and their application in practice alongside a working knowledge of how to comply with local, national and international research regulations. To manage a caseload of concurrent clinical studies following a range of complex clinical trial protocols and to contribute to the management of the local portfolio of clinical trials. To identify, screen and recruit participants into research studies according to the inclusion and exclusion criteria to ensure the effective achievement of study aims and monitoring of their condition throughout participation. To ensure that trial specific investigations are undertaken as required by the research protocol in order to establish eligibility and safety to enter the trial for its total duration.
act as a resource to the members of the MDT. To register/randomise participants into trials and to ensure that all clinical trial records, Case Report Forms (CRFs) and participant records are completed contemporaneously and maintained with a high degree of accuracy. These records may be in paper, optical or electronic form. To maintain accurate documentation of participant events in nursing/medical notes.
To identify barriers to recruitment to trials and ensure that the Network and R&D is aware of them. To support/action plans as required. To act as a primary contact point for clinical trial participants. To provide ongoing information, education and support to participants (and their significant others) regarding clinical trials.
Please refer to the Job Description for the full specification of responsibilities and requirements for this post

Please refer the Job description for details