Job summary
Clinical Research Nurse
Department: Research & Development
Band 6: £35,392- £42,618 per annum, pro rata if part-time
Fixed term contract until 10th February 2025
Hours: 37.5 hours per week, all MKUH roles will be considered for flexible working
This is an exciting opportunity for aregistered nurse, educated to degree level, with at least4yearsof clinical nursing experiencetoworkin research delivery. We are looking for someone who is adaptable, resourceful, patient centred andable to work in clinical settings as well asanoffice (IT, e-calendars, virtual meetings, data management).Prior experience in the Cancer specialty or research delivery prioritised.
The post holder willsupport the set-up, delivery, and follow-up of research studies across many specialities, gaining insight and experience into research governance, delivery and process which leads to evidence-based practice.
MKUHResearch and Development team is wellestablishedandhas achievedgreat successin recent years in recruiting patients to UKCRN trials,achievingseveral awards includingthe All-round High PerformingTeamandOutstandingResearch TeamLeader.We have a variety of studies across many specialities looking at cutting edge innovations and advancements aiming to improve patient outcomes.
Interviews on 12th January 2024.
For an informal discussion, please contact Claire Chama-Hall, Senior Research Practitioner & Cancer Lead - 85136
Main duties of the job
The post holder will work within the Research Team at Milton Keynes University Hospital NHS Foundation Trust, with a primary aim of promoting the entry of patients into clinical trials across the Trust. The post holder will work within the Generic Research team with a focus on DOCC, though working across other areas as work demands. The purpose of the job is to raise awareness of, deliver, and follow-up on clinical trials, increasing the number of patients recruited in line with National Institute for Health Research high level objectives.
Central to this role is the recruitment, education and monitoring of the patient entering a clinical trial. The maintenance of accurate and comprehensive records is an essential aspect of this post. The post holder will work closely with clinical teams and support departments as and where required, continually striving to improve quality of care and clinical outcomes. Delivery of the service level agreement with the Thames Valley and South Midlands Clinical Research Network (TVSMCRN) is an essential component of this role.
Contracts will be issued by Milton Keynes University Hospital on behalf of the Thames Valley and South Midlands Clinical Research Network on a fixed term contract. Extension subject to funding.
About us
You can expect a warm welcome at Milton Keynes University Hospital, our staff are friendly and welcoming. We listen to each other and work together to embed our Trusts values and behaviours. At MKUH we appreciate our staff and reward them with an outstanding benefits package including:
- Free on-site parking
- Free tea and coffee
- Great flexible workingopportunities
- Discounted gym membership
- Lease car scheme
- Generous annual leave and pension scheme
- On site nursery (chargeable)
- Extensive staff health and well-being programme
Milton Keynes University Hospital NHS Foundation Trust, in partnership with the University of Buckingham, is a University Teaching Hospital; we conduct research and teaching on site to improve the care of our patients. The hospital is undergoing significant investment, and we are proud to be rated good by the CQC. Visit our website to catch up on our latest news.
MKUH is committed to equal opportunities and improving the working lives of our staff and as such we offer a range of flexible working practices. We promote an inclusive workforce and encourage applications from applicants from all backgrounds.
We reserve the right to expire vacancies prior to the advertised closing date once a sufficient number of applications have been received.
MKUH uses identification scanning technology to confirm the authenticity of documents; all prospective employees of MKUH will have their original documents verified using this technology.
Job description
Job responsibilities
- Review each trial protocol to identify resource implications for Milton Keynes University Hospital NHS Foundation Trust.
- Ensure all regulatory approvals are in place prior to commencement of study. e.g. research ethics committee and Trust R&D permission.
Communication
- Promote trial involvement throughout the clinical and patient communities; Explain trials including complex trials in an unbiased sensitive way to emotive patients. Being able to display empathy and understanding
- Liaise and discuss trials including complex trial issues, with members of the MDT before, during and after the clinical trial
Education
- Attend the trial investigator / research nurse/practitioner meetings and conferences when required.
- Maintain awareness of current advances in medical treatments, research, and nursing practice (nurses only) and use this specialised knowledge to develop and maintain high standards of care for patients
Educating others
- Participate in the delivery of education and training programmes about clinical trials to all relevant healthcare staff with Milton Keynes University Hospital and TVSMCRN as appropriate.
- Develop and deliver education and training programs to all relevant healthcare staff within Milton Keynes University Hospital and TVSMCRN as appropriate.
Professional
- Act in accordance with the NMC Code of Professional Practice for Nurses, Midwives and Health Visitors and Scope of Professional Practice (nurses only).
- Maintain registration on the Clinical Research Practitioner directory and awareness of, and involvement in CRP initiatives.
Management
- Ability to work independently and be accountable for own professional actions. Self-manage all work areas and workload, seeking managerial supervision if required. Maintain own time schedule and ensure that all timelines are adhered to.
- Be aware of all Trust procedures and policies and collaborate with other healthcare professionals to ensure these are observed. Participate in the Development of Trust procedures and policies as required.
Please refer to the attached Job Description for more details on the role and responsibilities.
Job description
Job responsibilities
- Review each trial protocol to identify resource implications for Milton Keynes University Hospital NHS Foundation Trust.
- Ensure all regulatory approvals are in place prior to commencement of study. e.g. research ethics committee and Trust R&D permission.
Communication
- Promote trial involvement throughout the clinical and patient communities; Explain trials including complex trials in an unbiased sensitive way to emotive patients. Being able to display empathy and understanding
- Liaise and discuss trials including complex trial issues, with members of the MDT before, during and after the clinical trial
Education
- Attend the trial investigator / research nurse/practitioner meetings and conferences when required.
- Maintain awareness of current advances in medical treatments, research, and nursing practice (nurses only) and use this specialised knowledge to develop and maintain high standards of care for patients
Educating others
- Participate in the delivery of education and training programmes about clinical trials to all relevant healthcare staff with Milton Keynes University Hospital and TVSMCRN as appropriate.
- Develop and deliver education and training programs to all relevant healthcare staff within Milton Keynes University Hospital and TVSMCRN as appropriate.
Professional
- Act in accordance with the NMC Code of Professional Practice for Nurses, Midwives and Health Visitors and Scope of Professional Practice (nurses only).
- Maintain registration on the Clinical Research Practitioner directory and awareness of, and involvement in CRP initiatives.
Management
- Ability to work independently and be accountable for own professional actions. Self-manage all work areas and workload, seeking managerial supervision if required. Maintain own time schedule and ensure that all timelines are adhered to.
- Be aware of all Trust procedures and policies and collaborate with other healthcare professionals to ensure these are observed. Participate in the Development of Trust procedures and policies as required.
Please refer to the attached Job Description for more details on the role and responsibilities.
Person Specification
Qualifications and knowledge
Essential
- NMC Registered Nurse with relevant post registration experience to diploma level or equivalent
- Understanding of Research methods
Desirable
- Research qualification
- Knowledge of or undertaken Good Clinical Practice Training
Experience
Essential
- Relevant experience in a clinical setting
- Knowledge & experience in clinical research/clinical trials
Skills
Essential
- Able to organise work to meet deadlines and priorities
- Demonstrable ability to work on own initiative
- Ability to work as part of a team as well as on own initiative
- Able to analyse and interpret complex facts or situation
- Good IT skills including experience of using Microsoft Office software
- Attention to detail
- Ability to develop and implement quality control processes, to ensure the collection of high-quality data
Desirable
- Able to perform phlebotomy and cannulation
Personal and people development
Essential
- Demonstrable commitment to personal and professional development
Desirable
- Demonstrable commitment to educate others and share best practice
Communication
Essential
- Good communication and interpersonal skills, enthusiasm and a willingness to work closely and co-operatively with others
Desirable
Specific requirements
Essential
- Able to perform the duties of the post with reasonable aids and adaptations
Person Specification
Qualifications and knowledge
Essential
- NMC Registered Nurse with relevant post registration experience to diploma level or equivalent
- Understanding of Research methods
Desirable
- Research qualification
- Knowledge of or undertaken Good Clinical Practice Training
Experience
Essential
- Relevant experience in a clinical setting
- Knowledge & experience in clinical research/clinical trials
Skills
Essential
- Able to organise work to meet deadlines and priorities
- Demonstrable ability to work on own initiative
- Ability to work as part of a team as well as on own initiative
- Able to analyse and interpret complex facts or situation
- Good IT skills including experience of using Microsoft Office software
- Attention to detail
- Ability to develop and implement quality control processes, to ensure the collection of high-quality data
Desirable
- Able to perform phlebotomy and cannulation
Personal and people development
Essential
- Demonstrable commitment to personal and professional development
Desirable
- Demonstrable commitment to educate others and share best practice
Communication
Essential
- Good communication and interpersonal skills, enthusiasm and a willingness to work closely and co-operatively with others
Desirable
Specific requirements
Essential
- Able to perform the duties of the post with reasonable aids and adaptations
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).
