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Ready for an exciting career in research? The oncology and haematology research team oversees a diverse portfolio of research studies. Studies range from local academic studies to international multi-centre commercial clinical trials.
The role is based in the Clinical Research Facility within Sussex House in Brighton, covering core clinical hours 09:00 – 17:00, Monday to Friday.
This post is ideally suited to a Registered Nurse with a background in related specialties who wish to develop and broaden their experience, or for nurses with prior experience in research delivery. Relevant training will be given.
Please note that the role of the research nurse is significantly different from clinical services. You will spend much of your time at the computer setting up studies, preparing for visits, corresponding with participants and study representatives. You will be independently recruiting trial participants and running study visits, and ensuring data is collected thoroughly and accurately.
If you are a Registered Nurse who is motivated and enthusiastic, able to work both autonomously, as well as part of a small team, and have a strong interest in clinical research, we would like to hear from you. Informal visits to the Clinical Research Facility are essential to see if this role is a right fit for you. If a visit is not possible, please arrange a video or telephone call.
Having the knowledge and expertise to undertake the role of planning and co-ordinating a portfolio of clinical research trials. Must be highly self- motivated, accountable and able to work cohesively within a high-functioning team.
Responsible for the recruitment and consent of research participants, in conjunction with the Principal Investigator/Chief Investigator/ Research Team.
Upholding the principles of Good Clinical Practice, clearly explaining the research trial and ensuring that the participant is providing Informed Consent.
Excellent communication, preparation and attention to detail is essential in order to liaise with participants, clinicians, trial sponsors and research colleagues.
Assess patients, plan, implement and manage care. Build relationships and act with a high degree of professionalism.
Carry out specialist nursing procedures and treatments as directed by the research protocols.
Provide specialist advice and education clearly to patients/participants and carers with regard to the clinical research and specialist areas.
Comfortable navigating new software.
Will be required to supervise other members of the nursing team and support staff.
To work flexibly across various clinical environments. Able to prioritise, manage competing priorities, and problem solve independently. This role requires working with self-initiative and expanding your practice to learn about new specialties.
Responsible and accountable for the timely coordination and delivery of complex participant-centred clinical research trials, including the identification, recruitment and subsequent treatment, care and follow up of research participants.
Be highly skilled and competent in the comprehensive assessment of patients using theoretical knowledge and a wide range of experience to assess needs and administer care and treatment in accordance with research protocols. Responsive in the event of clinical adverse events/reactions.
Co-ordinate interventions which may include other disciplines, multidisciplinary team meetings, integrated teams within the hospital and in the community in relation to the research protocols and care pathways of participants.
Ensure all documentation and data are completed in a timely and accurate manner and that all information is stored and maintained appropriately. Able to understand and adhere to complex protocols.
Please see Job Description and Person Specification for full details.
We welcome applications from those who currently hold a UK NMC registration. If you currently hold an overseas nursing qualification and require sponsorship we are not currently direct hiring Internationally Qualified Nurses.