Job summary
Clinical Research Nurse
Department: Research & Development
Band 6: £35,392- £42,618 (pro rata if part-time) Fixed term contract: 9 months
Hours: 37.5 hrs/week
Two roles (1 x 6mths & 1 x 9mths - Maternity Cover)
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).
The post holder willsupport the set-up, delivery, and follow-up of research studies across various specialities, hence the requirement for a sound clinical base. Gaining insight and experience into research governance, delivery and process which leads to evidence-based practice this is a great addition to your career.
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 18th September 2024.
For an informal discussion, please contact Zoey - zoey.horne@mkuh.nhs.uk, Senior Research Nurse - 01908 995927
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
Nurses and midwives lead the charge in acknowledging the significance of every voice, boasting an impressive score of 7.19/10 in the theme "We each have a voice that counts."(NHS Staff Survey 2023)
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.
Job description
Job responsibilities
Implement, develop and facilitate the running of trials as part of the research team within Milton Keynes University Hospital, as directed by the Research & Development Department and involve clinicians, in order to achieve the objectives of the TVSMCRN outlined above.
This will include:
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.
Identify eligible patients for trials (by attending clinics and multidisciplinary team (MDT) meetings etc. and assessing clinical condition of patient in detail).
Ensure that patients are advised of and understand fully all the details of the trial.
With the appropriate Consultant obtain informed consent from the patient. For identified trials, the Research Nurse/Practitioner can independently obtain written informed consent from the patient ensuring that GCP guidelines are strictly adhered to. Be responsible for obtaining randomisation status, treatment allocation and collection of follow up data, including quality of life questionnaires. Be responsible for maintaining trial information and data in the patient notes.
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.
Be available to deal with patients / carers queries and concerns. Take responsibility for explaining trials including complex trial procedures and treatments, answering in a manner appropriate to the patient.
Liaise with the relevant support services e.g. designated pharmacist, concerning the running of the 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.
Participate in formal and informal teaching programmes, study days and educational programmes within the Trust, as arranged by TVSMCRN/Divisions and elsewhere as appropriate.
Identify personal training requirements and initiate appropriate training.
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.
Disseminate research findings by developing and presenting posters / research papers for meetings, conferences, and publication. Circulate trial information and carry out presentations locally.
Please refer to the job description for further details.
Job description
Job responsibilities
Implement, develop and facilitate the running of trials as part of the research team within Milton Keynes University Hospital, as directed by the Research & Development Department and involve clinicians, in order to achieve the objectives of the TVSMCRN outlined above.
This will include:
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.
Identify eligible patients for trials (by attending clinics and multidisciplinary team (MDT) meetings etc. and assessing clinical condition of patient in detail).
Ensure that patients are advised of and understand fully all the details of the trial.
With the appropriate Consultant obtain informed consent from the patient. For identified trials, the Research Nurse/Practitioner can independently obtain written informed consent from the patient ensuring that GCP guidelines are strictly adhered to. Be responsible for obtaining randomisation status, treatment allocation and collection of follow up data, including quality of life questionnaires. Be responsible for maintaining trial information and data in the patient notes.
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.
Be available to deal with patients / carers queries and concerns. Take responsibility for explaining trials including complex trial procedures and treatments, answering in a manner appropriate to the patient.
Liaise with the relevant support services e.g. designated pharmacist, concerning the running of the 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.
Participate in formal and informal teaching programmes, study days and educational programmes within the Trust, as arranged by TVSMCRN/Divisions and elsewhere as appropriate.
Identify personal training requirements and initiate appropriate training.
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.
Disseminate research findings by developing and presenting posters / research papers for meetings, conferences, and publication. Circulate trial information and carry out presentations locally.
Please refer to the job description for further details.
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
- Minimum of 2 years' 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
- Minimum of 2 years' 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
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
