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The Trust is continuing to build its portfolio in order to develop research locally and improve access to clinical trials for the people of Warrington and Halton. The benefits of active participation in research are well recognised in leading to successful outcomes for patients as well as helping ensure our clinical staff stays abreast of the latest possible treatment options. The post holder will be a member of an established team and responsible for co-ordinating an agreed portfolio of NIHR research studies. The successful applicant may be an experienced research nurse or a nurse looking to move into research as full training will be given. Key responsibilities of the post include: assisting in study set up, identifying patients through screening notes, collecting data, interviewing, supporting, and monitoring patients and data entry. It is anticipated that the post-holder will be based at Warrington although dependent upon the needs of the service may also be required to work from Halton. Funding for this post is being provided by the Regional Research Delivery Network.
To be responsible for the day-to-day management of, and patient recruitment to, all studies assigned to you as a generic research nurse. • To work on a daily basis with minimum supervision as part of the research team • To identify, screen, interview patients and recruit them into the appropriate studies. • To co-ordinate and carry out patient visits in accordance with study protocols, including coordinating special tests in other departments, collection of data, coding, data entry, and patient support. • To ensure that the patient’s health and safety are paramount in all procedures that take place for trial purposes. • To ensure clinical and research documentation and record keeping is completed accurately and efficiently in accordance with NMC and EU Directive (ICH GCP) Guidelines. • To co-operate with and support other Research Nurses within the department. • To understand the relevance of research to health care delivery and be able to identify • To develop the skills of other staff by identifying needs through observation and ensuring participation, practice and relevant education. • To participate in the education and development of staff/students, e.g. clinical supervision and ensure that all personnel are adequately informed about and comply with all details of the trials.
To contribute to all aspects of the planning, conduct and reporting of all clinical trials and in-house studies in the relevant field.
FULL JOB DESCRIPTION ATTACHED.