Clinical Research Nurse
| Posting date: | 12 November 2025 |
|---|---|
| Salary: | £38,682.00 to £46,580.00 per year |
| Additional salary information: | £38682.00 - £46580.00 a year |
| Hours: | Full time |
| Closing date: | 22 November 2025 |
| Location: | Norwich, NR4 7UY |
| Company: | NHS Jobs |
| Job type: | Contract |
| Job reference: | C9234-25-0660 |
Summary
Fixed term contract/secondment opportunity for 23 months If you are considering applying for this post on a secondment basis, please discuss with your Line Manager prior to applying to ascertain whether this could be supported. 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. To attend multi-disciplinary team meetings (MDT), and appropriate clinics, to screen and recruit new participants, and to 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 the clinical trial participant. To provide ongoing information, education and support to participants (and their significant others) regarding clinical trials. Please see the attached job description for full details. Interview W/C 1st December (to be confirmed).