Job summary
This post is part of a growing team of research nurses and practitioners working in the research and development (R&D) team at CPFT. This is a part-time 22.5 hours per week, 12-months fixed term contract post.
The post has been specifically designed to be based at the Cavell Centre, offering research delivery support to CPFT service users and staff in the north of the county out of the newly initiated research facility at the Cavell Centre. The primary base will, therefore, be the Cavell Centre, Peterborough with an expectation to provide support at the Windsor Research Unit (Fulbourn hospital, Cambridge) on a business needs basis.
Main duties of the job
The post holder will be responsible for the day to day running of studies and clinical trials across Cambridge and Peterborough. These studies will cover four specialities: Mental health, Dementia, Physical health/community and rare diseases. The post holder will be coordinating patient care during research studies with responsibility for conducting clinical activities education and monitoring of study subjects through care pathways.
The post holder will support more junior clinical research nurses/ clinical research practitioners, assisting them to develop their clinical research skills thorough education and training.
About us
Cambridgeshire and Peterborough NHS Foundation Trust is a health and social care organisation dedicated to providing high-quality care with compassion to improve the health and wellbeing of the people we care for, as well as supporting andempowering them to lead a fulfilling life.
Our clinical teams deliver many NHS services, not only via inpatient and primary care settings, but also within the community. These services include children's, adult and older people's mental health, forensic and specialist mental health, learning disabilities, primary care and liaison psychiatry, substance misuse, social care, research and development.
To achieve our goal, we look to recruit high-calibre candidates who share our vision and values. As an equal opportunities employer, we encourage applications from all sectors of the community, particularly from under-represented groups including people with long term conditions and members of our ethnic minority and LGBTQ+ communities.
Please be advised we reserve the right to close adverts earlier than the closing date should we receive sufficient applications.
Regrettably, we cannot offer sponsorship for all our job roles. If you apply for a role that we cannot offer sponsorship for, unfortunately, your application form will be rejected from the process.
For further information on CPFT, please visit our website at www.cpft.nhs.uk
Job description
Job responsibilities
Please refer to the attached job description and person specification for full details of responsibilities.
To identify potential participants from clinical services, community services, university and NHS databases, specialist clinics, third sector organisations, schools and other access routes, for RDN portfolio studies and clinical trials.
To work with the clinical teams to map the patient pathway for specific trials, performing cognitive assessments, psychological assessments, ECGs, physical examination and phlebotomy and associated processing.
To deliver and promote clinical trials and other research studies within the trust.
To ensure day to day practice reflects the highest standards of governance, clinical effectiveness, safety and patient experience.
To work collaboratively with other colleagues to ensure all studies are delivered on time and target and are delivered in accordance with the requirements of the study protocol.
To safely administer all treatments and medications within the context of a clinical trial
To be responsible for accurate and timely completion of case report forms (CRFs). Accurate and timely completion of all study-related activities, electronically and/or in paper format.
To undertake all aspects of the study protocol and research pathway, including obtaining informed consent, performing all assessments and cognitive testing and aspects of physical examination, and arranging and undertaking follow-ups.
To take and process blood samples required and ensure safe and appropriate storage of specimens.
To maintain accurate patient records and ensure all relevant information is documented within the patients medical notes and study source documentation.
To support carers through the study process, ensuring those involved are well informed.
To facilitate delivery of the study procedures in line with the study protocol and ensure that all travel arrangements, hotels etc. are organised for study participants in advance of their arrival.
Please note for this role you will be required to travel independently around the county meeting strict time deadlines. You will need to hold a full UK driving licence* and have use of a vehicle. You cannot use public transport for this role as this is not a reliable form of transport and will not allow you to meet service needs. Please confirm in your application that you meet the specified criteria.
Job description
Job responsibilities
Please refer to the attached job description and person specification for full details of responsibilities.
To identify potential participants from clinical services, community services, university and NHS databases, specialist clinics, third sector organisations, schools and other access routes, for RDN portfolio studies and clinical trials.
To work with the clinical teams to map the patient pathway for specific trials, performing cognitive assessments, psychological assessments, ECGs, physical examination and phlebotomy and associated processing.
To deliver and promote clinical trials and other research studies within the trust.
To ensure day to day practice reflects the highest standards of governance, clinical effectiveness, safety and patient experience.
To work collaboratively with other colleagues to ensure all studies are delivered on time and target and are delivered in accordance with the requirements of the study protocol.
To safely administer all treatments and medications within the context of a clinical trial
To be responsible for accurate and timely completion of case report forms (CRFs). Accurate and timely completion of all study-related activities, electronically and/or in paper format.
To undertake all aspects of the study protocol and research pathway, including obtaining informed consent, performing all assessments and cognitive testing and aspects of physical examination, and arranging and undertaking follow-ups.
To take and process blood samples required and ensure safe and appropriate storage of specimens.
To maintain accurate patient records and ensure all relevant information is documented within the patients medical notes and study source documentation.
To support carers through the study process, ensuring those involved are well informed.
To facilitate delivery of the study procedures in line with the study protocol and ensure that all travel arrangements, hotels etc. are organised for study participants in advance of their arrival.
Please note for this role you will be required to travel independently around the county meeting strict time deadlines. You will need to hold a full UK driving licence* and have use of a vehicle. You cannot use public transport for this role as this is not a reliable form of transport and will not allow you to meet service needs. Please confirm in your application that you meet the specified criteria.
Person Specification
Education / Qualifications
Essential
- NMC Registered Nurse
- ICH GCP Training
Desirable
Experience
Essential
- Experience as a research nurse working in a clinical research environment
- Experience of recruiting to research studies including clinical trials in a healthcare setting
- Experience of working with people with mental health conditions and dementia
Skills & Abilities
Essential
- Experience in performing cognitive assessments
- Ability to critically read a research study protocol, understand the methodology and its practical application
- Ability to engage and recruit patients into clinical trials.
- Pertinent clinical skills including venepuncture
Desirable
- Experience of performing Mental Capacity assessments
- Experience in conducting supervision and appraisals
Knowledge & Understanding
Essential
- Knowledge of the legislation relating to information governance, confidentiality requirements and data protection.
- Knowledge of Research Governance Framework and Good Clinical Practice Guidelines
- Good working knowledge of Mental Capacity Act
- Understanding of the needs and capabilities of people with dementia, neurodegenerative disorders and mental health conditions
Other
Essential
- Ability to travel independently (many research visits will take place in patients' homes or off site) and attend conferences / training away from home.
- Good standards of written and verbal communication
Person Specification
Education / Qualifications
Essential
- NMC Registered Nurse
- ICH GCP Training
Desirable
Experience
Essential
- Experience as a research nurse working in a clinical research environment
- Experience of recruiting to research studies including clinical trials in a healthcare setting
- Experience of working with people with mental health conditions and dementia
Skills & Abilities
Essential
- Experience in performing cognitive assessments
- Ability to critically read a research study protocol, understand the methodology and its practical application
- Ability to engage and recruit patients into clinical trials.
- Pertinent clinical skills including venepuncture
Desirable
- Experience of performing Mental Capacity assessments
- Experience in conducting supervision and appraisals
Knowledge & Understanding
Essential
- Knowledge of the legislation relating to information governance, confidentiality requirements and data protection.
- Knowledge of Research Governance Framework and Good Clinical Practice Guidelines
- Good working knowledge of Mental Capacity Act
- Understanding of the needs and capabilities of people with dementia, neurodegenerative disorders and mental health conditions
Other
Essential
- Ability to travel independently (many research visits will take place in patients' homes or off site) and attend conferences / training away from home.
- Good standards of written and verbal communication
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.
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present 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) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
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.
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present 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) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
