Job summary
We are looking for afull time Band 6 Clinical Research Nurse to join our busy research team overseeing a portfolio of clinical 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 HouseBrighton.
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 Registered 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.
Main duties of the job
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.
About us
Working for our organisation
At UHSussex, diversity is our strength, and we want you to feel included to help us always deliver Excellent Care Everywhere, as shown in our Outstanding for Caring CQC rating. Your uniqueness and experiences will be part of our creative and innovative community where everyone is encouraged to succeed. We have a range of staff networks to help break down barriers, and can offer abuddy to help new members settle in. We're proud to be a Disability Confident Employer (Level 3) and a Veteran Aware Trust.
Candidate Pack
Job description
Job responsibilities
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.
Job description
Job responsibilities
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.
Person Specification
Experience/ Qualifications/ Skills
Essential
- First Level Nurse Registration
- First degree or equivalent experience, with significant post registration experience in one or more areas of the desired portfolio
- Mentorship Qualification e.g. Practice Supervisor Practice Assessor Preparation Programme, Mentorship Programme, ENB 998, Practice Teacher qualification or equivalent
- Good Clinical Practice certificate
- Post-registration experience
Desirable
- Research experience/interest
- IT skills
- ICH GCP Certificate
- Demonstrates training of others
- Caseload management
Equality, Diversity, and Inclusion
Essential
- Evidence of having undertaken own development to improve understanding of equalities issues
- Evidence of having championed diversity in previous roles (as appropriate to role)
Person Specification
Experience/ Qualifications/ Skills
Essential
- First Level Nurse Registration
- First degree or equivalent experience, with significant post registration experience in one or more areas of the desired portfolio
- Mentorship Qualification e.g. Practice Supervisor Practice Assessor Preparation Programme, Mentorship Programme, ENB 998, Practice Teacher qualification or equivalent
- Good Clinical Practice certificate
- Post-registration experience
Desirable
- Research experience/interest
- IT skills
- ICH GCP Certificate
- Demonstrates training of others
- Caseload management
Equality, Diversity, and Inclusion
Essential
- Evidence of having undertaken own development to improve understanding of equalities issues
- Evidence of having championed diversity in previous roles (as appropriate to role)
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
