About CPFT
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 and empowering 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.
About the role
In this exciting role, the post holder will travel to mental health clinics throughout Cambridgeshire and Peterborough NHS Foundation Trust (CPFT) to discuss the QUEST trial with community mental health service users, and recruit patients with a diagnosis of borderline personality disorder. The post holder will also be required to travel independently around the county, hold a full UK driving licence and have use of a vehicle; public transport is not acceptable. Full training will be provided.
The post holder will collect data for the project in clinics or participant homes, involving the Zanarini Rating Scale for Borderline Personality Disorder (ZAN‑BPD), Structured Clinical Interview for DSM‑V Personality Disorders (SCID‑5‑PD) and a range of other measures. Maintaining good working relationships with service users, carers, clinic staff and other stakeholders will be key to the success of the project.
The successful candidate should be organised, capable of independent work, with strong interpersonal skills and a good awareness of mental health difficulties. The post holder will be based in the CPFT R and D department, working alongside a vibrant research team and supported by the study Chief Investigator, Principal Investigator and the QUEST study team, research and delivery staff and clinical services to assist with the successful delivery of the study and achievement of local and national targets in relation to research performance.
Key Responsibilities
* Assist in the set‑up and facilitation of the research project.
* Maintain and manage an external database of quantitative data, anonymise data, input data into the database and keep it up to date.
* Approach potential research participants using a variety of communication formats, in order to engage them in the research study.
* Carry out any relevant psychometric test materials and structured/semi-structured interviews whilst ensuring the safety and comfort of participants and yourself.
* Follow‑up research participants at agreed intervals where indicated.
* Be aware of the psychological/emotional needs of research participants, responding and reporting appropriately.
* Ensure that research procedures (including consent processes and follow‑up) are carried out according to the approved protocol and the UK policy framework for health and social care research.
* Conduct reviews of electronic patient clinical notes, extracting and coding data for research purposes.
* Score relevant tests, make data anonymous and enter data into the study database.
* Ensure safe storage of paper data.
* Arrange briefings for teams as appropriate and undertake presentations if required on the nature and requirements of the study.
* Assist the trial managers and other members of the study team with the general delivery of the study.
* Liaise with the study sponsor, clinicians and research collaborators.
* Organise data collection opportunities associated with the research study.
* Complete screening logs to capture data on participants approached and consented.
* Attend training and ongoing supervision for the trial as developed and delivered by the Central Management Team and supported by the site clinical Principal Investigator.
* Enter and check research data.
* Undertake advance planning to meet deadlines for formal study monitoring and study milestones (e.g., participant recruitment, data collection and data analysis).
* Support writing papers for publication during dissemination of results (if requested).
* Ensure compliance with research and clinical governance guidelines, training, data protection and ethical requirements.
Equality and Diversity
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.
Other Information
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.
Please refer to the attached job description and person specification for full details of responsibilities.
Further information on CPFT: www.cpft.nhs.uk
This advert closes on Wednesday 19 Nov 2025.
#J-18808-Ljbffr