Research Nurse

The Trust is looking to recruit a  1.0 WTE research nurse.

The aim of this post is to allow opportunity for a high calibre nurse to develop their skills both clinically and in the field of research. We aim to equip the individual with the skills and qualifications to become a strong autonomous research practitioner within their specialist clinical field.

The post holder will be responsible for assisting the Trust with its commitment to a sustained and dramatic increase in recruitment of patients into research studies.  For this role the post holder will specifically be concerned with recruitment to the gynaecology research studies. The individual will also be responsible for assisting the Research & Development office with feasibility and set up of new research.

The Trust has a diverse and growing portfolio of research its research practitioners are recruiting to, some of which overlap with other speciality areas.

Internal secondments may be considered but applicants MUST SEEK APPROVAL from their substantive clinical line manager FIRST.

Although the role is advertised at a Band 6,  we would also welcome applications from individuals who do not fully meet the research experience criteria.  Such an individual would have the opportunity to be employed in a Band 5 position, to allow for the appropriate training to take place in order to meet the role competencies.

To support the operational management of gynaecology research studies.

To contribute to all aspects of the planning, conduct and reporting of the portfolio clinical research trials and studies.

To be responsible for the day-to-day management of, and patient recruitment to designated research studies.

To work on a daily basis with minimum supervision as part of the research team.

To ensure that all clinical research activity is ICH GCP compliant and conducted in accordance with the agreed protocols.

To maintain a high standard of patient care in line with Trust and R&D procedures and protocols and in accordance with the UK Policy Framework for Health and Social Care Research.

To prioritise research activity as necessary thus ensuring recruitment targets are met.

To ensure that all data is collected and managed effectively and accurately.

Act as a focus for research communication within the Trust and with external partners including the Clinical Research Network.

To disseminate information to colleagues in respect of the research studies taking place within the clinical areas.

Liaison with research sponsors and multi-disciplinary research teams.

To give advice on the organisation and management of the research in progress.

To identify and screen eligible patients for participation in the research studies.

To facilitate the informed consent and recruitment of research participants.

To work with staff to develop strategies to overcome barriers to recruitment.

To be aware of ethical considerations of research and act as the patient’s advocate at all times.

To be fully conversant with the requirements of the clinical trial protocol in relation to patient management, data collection and safety reporting.

To carry out the collection, processing and shipping of biological specimens according to protocol requirements and follow-up appropriately.

Maintain accurate records and undertake the Data management including the use of data software packages.

Dissemination and publication of research findings.

Actively contribute to activities, events and training within the research teams.

To contribute to evidence based practice at a clinical level and maintain overall standard of care for patients at all times.