Employer: James Paget University Hospitals NHS Foundation Trust
Employer type: NHS
Site: James Paget University Hospital
Town: Great Yarmouth
Salary: £29,970 - £36,483 per annum, pro rata
Salary period: Yearly
Closing: 17/11/2024 23:59
Multispecialty Clinical Research Support Nurse/AHP/Research Practitioner
NHS AfC: Band 5
The James Paget University Hospitals NHS Foundation Trust serves a population of around 250,000 people in the Great Yarmouth, Lowestoft and Waveney areas. The Trust provides an integrated hospital and community children’s service.
Patient and staff experience is important to us and these are the behaviours we live by:
* Putting patients first
* Aiming to get it right
* Recognising that everybody counts
* Doing everything openly and honestly
‘Prior consideration will be given to NHS At Risk staff within East of England'
Job overview
Do you have a passion for improving patient care and treatment pathways? Then come and join our established and dynamic research team where you will spend your time as an essential part of our team.
Research is an integral part of healthcare and Clinical research nurses and AHPs play a vital role in delivering clinical research, and ultimately improving patient care and treatment pathways.
An opportunity has arisen within the Research and Development Department for a Multispecialty Clinical Research Support Nurse/AHP/Research Practitioner to support the Multispecialty Research Team. This is a Band 5 post, initially fixed for 12 months, with the potential for extension dependent upon continued funding.
We will consider a secondment for this position.
Main duties of the job
We are looking for a highly motivated team player who is interested in supporting research delivery. Ideally you will have Ophthalmology experience or experience working in a clinical research environment and knowledge of the research process in the NHS. Excellent IT skills are also a requirement for this role.
The post holder will be involved in the day-to-day running of clinical trials which involves recruitment, treatment, monitoring, and collection of blood for pharmacokinetic / pharmacodynamics studies, and the provision of support to the patients involved. You will also be expected to liaise with study sponsors and other research partners.
Working for our organisation
This post offers the opportunity to develop your clinical and research skills, and to be part of a growing research community. Full research training and continuing professional development is considered a high priority within the team and will be provided from induction onwards.
Delivering relevant, important clinical research for our patients is all part of a day’s work in our friendly Research and Development Team at the James Paget University Hospital NHS Foundation Trust.
Detailed job description and main responsibilities
Main duties and Responsibilities
Key research areas:
* Work autonomously within operating procedures and study protocols to manage his/her caseload of patients, whilst working as part of a multi-disciplinary team.
* Interview, recruit, receive informed consent and support patients and carers in observational trials/studies. This involves educating patients on the trials involved, explaining the advantages and disadvantages of taking part in observational studies/trials, whilst remaining unbiased at all times. Assess patients as required by trial protocols relating to inclusion and exclusion criteria and study related tasks.
* Enhanced clinical skills: ability to take blood samples, vital sign measurement (including temperature, blood pressure, pulse and respiratory rate) and know how to act upon significant results. Pregnancy testing.
* Maintain high quality patient records and ensure all relevant information is documented in the patient’s notes and relevant research case report and other forms are completed to Good Clinical Practice (GCP) standards.
* Provide continuity of care for patients and their carers throughout the trial programme. Provide non-clinical advice and support as appropriate to patients and carers. Ensure the provision of optimal patient care by alerting appropriate clinical colleagues when referral to other members of the MDT may be required.
For both observational and interventional research trials/studies.
* Attend MDT meetings and liaise with MDT members to establish procedures for the safe and smooth running of clinical trials and act as a resource and contact point in matters concerning trial patients and trial protocols.
* Screen for and identify suitable patients for trials by assessing patients against criteria defined by all trial protocols. Arrange and where appropriate perform, investigations required to establish eligibility and safety for trial/study entry.
* Review patient records, identify source data, accurately collect and complete a range of complex and more simplistic data collection forms both electronically and in paper format, in timeframes required by both the study Sponsor and GCP.
* Administer questionnaires/diaries to patients, provide instruction and subsequent collection.
* Perform consistency checks on data collected for each patient throughout their trial journey. Resolve inconsistencies and respond to data collection queries.
* Responsible for identifying safety reporting (either from communicating with patients/relatives, carers or clinical colleagues, or from investigating medical records) and reporting these within both GCP and individual study deadlines.
* Design forms to capture source data; the forms will be specific to each trial but will have an agreed format.
* Design and maintain spreadsheets/databases to track patient journeys in trials/studies. The spreadsheets/databases may be used by all members of the research team as an information and/or planning resource.
* Responsible for ensuring trial/study participants adhere to trial protocols, for example, clinic appointments within correct windows (including the pre-planning of visit dates and booking of appointments).
* Provide support to the lead study nurse for interventional studies for clinical and non-clinical tasks.
* Ensure that trials/studies are conducted according to the Research Governance Framework, EU Clinical Trials Directive EU2001/20EC and EU GCP Directive 2005/28/EC.
* Maintain clinical trial site files to ensure a complete audit trail for trials.
* Be part of the departmental research team in the review of trial/study protocols and identify resource implications for the site.
* Assist with trial set-up, liaising with clinicians, supporting departments, other healthcare professionals and trials units, as required.
* To act as a direct contact for clinical trial/study patients.
To help identify barriers to recruitment and performance, communicating these to the study team and Senior Clinical Research Nurse.
Person specification
Qualifications
* Evidence of recent short courses and/or study days on research
* GCP Certificate
* Degree in health-sciences or willingness to work towards
* Registered Nurse/AHP on the appropriate part of the NMC/HCPC register
Skills
* Ability to take blood and perform vital signs (Blood pressure, temperature, pulse, respiratory rate), pregnancy testing and blood glucose measurements
* Excellent IT skills (Microsoft Office inc word, excel, powerpoint, Diary management etc)
* Able to prioritise workload and meet deadlines within a challenging environment
* Flexible and responsive to change
* Ability to be able to lead on an observational-only research study
* Analysis of study data
Experience
* Recent experience working in a busy NHS clinical or research environment
* Experience of dealing with difficult situations and coming to resolutions
* Experience working in Ophthalmology
* Understanding of research pathway from idea to delivery and close-out
* Knowledge of ethical and quality standards applicable to clinical trials
Communication and relationship skills
* Able to communicate concerns in a timely manner
* Effective oral and written communication skills
* Ability to handle sensitive situations and challenging attitudes
* Demonstrable experience of communicating with patients/carers
* Demonstrable experience of communicating with Research Study Sponsors or external companies
The James Paget University Hospitals NHS Foundation Trust recognises the requirement to promote health and reduce ill-health. The Trust is committed to the principles of improving working lives through a number of initiatives such as job share, flexible working and the development of a culture of openness and transparency. The Trust is committed to ensuring that no job applicant or employee receives less favourable treatment on the grounds of their age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion or belief, sex, and sexual orientation.
‘Prior consideration will be given to NHS At Risk staff within East of England'
Tier 2 Sponsorship: We are pleased to consider applicants who require Tier 2 sponsorship to work in the UK but it is unlikely that we would be able to appoint if a suitably qualified, experienced and skilled UK/Right to work candidate is available. Applying for entry clearance into the UK, must provide a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) will also be subject to this requirement.
Please check your account regularly under “My Applications” to view the progress of your applications. If you do not hear from us within 4 weeks, please assume your application has been unsuccessful.
In submitting an application form, you authorise the Trust to confirm any previous NHS service details via the Inter Authority Transfer (IAT) process.
Please note that should we experience a high level of interest in this post, the vacancy may be closed prior to the stated closing date.
Employer certification / accreditation badges
You must have appropriate UK professional registration.
This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.
For further information or informal chat please call:
Helen Sutherland, Senior Clinical Research Nurse, Tel: 01493 453606 [emailprotected]
Martine Foyster, Multispecialty Clinical Research AHP, Tel: 01493 453607 [emailprotected]
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