Research Nurse


Company:	NHS Jobs
Salary:	Negotiable
Hours:	Full-time
Location:	Blackburn, BB2 3HH
Job type:	Contract
Posting date:	30 Oct 2026
Closing date:	13 Nov 2026

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Summary

To ensure all research studies carried out are registered and approved by the NHS Organisation and have a favourable opinion from the Research Ethics Committee. To provide support to clinical investigators in obtaining approval from the NHS Organisation and favourable opinion from Research Ethics Committees. To become familiar with each research protocol and its application in practice including procedures and documentation to ensure safe and accurate conduct and recording within the study. To undertake study feasibility, wider clinical staff training/ awareness of new studies. To identify, screen and recruit eligible participants into research studies according to specific protocols and guidelines To co-ordinate recruitment for a local portfolio of clinical studies across participating sites/practices. To provide information, education, and support to clinical team members, regarding clinical studies To facilitate the informed consent process bearing in mind the clinical status of patients ensuring the following is accounted for:- - The patient (and significant others) fully understands the nature of the clinical trial. - The patient is aware that entry into the trial is voluntary, and they can withdraw at any point without prejudice. The patient is aware of any extra procedures required by the trial. The consent form is completed accurately and filed as required. To disseminate up to date information, protocol amendments etc. to personnel working on research projects To be responsible for monitoring trial data/accrual in clinical studies and forwarding it in a timely manner to the trial co-ordinating centre and the Trust Research and Development Department. Liaise with clinical trial personnel as necessary. To identify barriers to recruitment to studies and ensure that the Research and Development Manager is aware of them. Identify and implement action/plans as required. To participate in study monitoring both externally and internally in line withresearch governance requirements Where delegated to do so, set up and maintain study site files in accordance with ICHGCP and Trust SOPs

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