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We are looking for a full time Band 6 Clinical Research Nurse to join our busy research team overseeing a portfolio of research studies across multiple specialities within the Trust. These specialities include, but are not limited to neurology, critical care, orthopaedics and surgeries.
The role will predominately be based in the Clinical Research Facility within Sussex House Brighton.
You will coordinate and support a range of clinical trials, including local academic studies and international multi-centre commercial clinical trials adhering to the principles of Good Clinical Practice in research.
Excellent communication, education and attention to detail is essential to liaise with participants, clinicians, sponsor representatives and research colleagues.
This post is ideally suited to a nurse with a background in related specialties who wishes to develop and broaden their experience. Relevant training will be given.
If you are a Registered Nurse who is motivated and enthusiastic, able to work autonomously and as part of a team who has an interest in clinical research we would like to hear from you. Informal visits are recommended and encouraged.
This role is eligible for visa sponsorship under the UK Visas & Immigration (UKVI) Skilled Worker route however sponsorship can only be provided where applicants meet the specific requirements set by UKVI, including the relevant skill and salary thresholds (£25000), and any role-specific criteria.
Has the knowledge and expertise to undertake the role of planning and co-ordinating a portfolio of clinical research trials.
Responsible for the recruitment of research patients/participants, in conjunction with the Principal Investigator/Chief Investigator/ Research Team.
Assess patients, plan, implement and manage care.
Carry out specialist nursing procedures and treatments as directed by the research protocols.
Provide specialist advice to patients/participants and carers with regard to the clinical research and specialist areas.
Will be required to supervise other members of the nursing team and support staff.
To work flexibly.
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.
Work on own initiative to undertake a wide range of duties relating to clinical research, backed up by professional skills and knowledge, including being able to respond in the event of clinical adverse events/reactions.
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.
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.
Please see Job Description and Person Specification for full details.