Neidio i'r prif gynnwys
Arhoswch, yn llwytho

Crynodeb o'r swydd

Prif leoliad
Cardiovascular
Gradd
NHS AfC: Band 5
Contract
Parhaol
Oriau
Rhan-amser - 22.5 awr yr wythnos (Part time)
Cyfeirnod y swydd
358-7330200-COR
Cyflogwr
University Hospitals of Leicester NHS Trust
Math o gyflogwr
NHS
Gwefan
GGH
Tref
Leicester
Cyflog
£31,049 - £37,796 per annum
Cyfnod cyflog
Yn flynyddol
Yn cau
11/09/2025 08:00

Teitl cyflogwr

University Hospitals of Leicester NHS Trust logo

Cardiovascular Research Nurse- Band 5

NHS AfC: Band 5

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But they shouldn’t replace your own responses or be used to write the application for you.

Relying too much on AI can negatively impact your chances of success, because automatically generated answers:

  • might not be specific or relevant enough to address the criteria in the recruitment profile
  • often seem generic and not personalised enough – an AI response won’t show your unique voice and perspective
  • could misrepresent information about you, such as your qualifications, skills and experience

We monitor applications for any behaviour that could create an unfair advantage, and we check all references carefully. You are likely to be tested on your experience at interview, so be honest and make sure all the information in your application is correct.

Trosolwg o'r swydd

An exciting opportunity has arisen for a Band 5  Research Nurse,  with a cardio/vascular background, to join our friendly and supportive team. 

 We are a well-established team running many research projects involving all aspects of cardiovascular care with an emphasis on Vascular.

We are looking to appoint a confident, highly organized and self-motivated Research Nurse. You will need to have excellent communication, interpersonal and organizational skills.

Prif ddyletswyddau'r swydd

  • Manages a personal caseload of clinical trials and patients with supervision/mentoring from Principle Investigators/senior research nurses/research nurses.

  • To ensure all work is undertaken in line with the research protocol, ICH-GCP and Research Governance guidelines

  • Identifies, screens and recruits patients for the clinical trial using agreed protocols in accordance with ICH-GCP and Research Governance

  •  Provides education and support for patients in research trials

  •  With supervision, work with the lead clinician to evaluate clinical trial proposals, identifying potential patient populations and evaluating cost implications of the trial. 

  •  With supervision participate in set-up/initiation/monitoring visits, site audits and study close-down meetings carried out by sponsoring organisations and regulatory authorities.

  •  Provide on-going audit reports as required by the trial protocols and Research & Innovation department/ethics committee.

  •  Responsible for resolving data queries raised by sponsoring organisations.

  • Demonstrates commitment to the role of patient advocate for patients considering or participating in clinical trials

  • Act as a resource for ward based nurses wishing to undertake research once competencies have been achieved

Gweithio i'n sefydliad

Our new strategy, developed with the support and feedback of colleagues, patients, and partners, is our compass for the next seven years (2023-2030).

We have four primary goals: 

  • high-quality care for all, 
  • being a great place to work, 
  • partnerships for impact, and 
  • research and education excellence

And we will embed health equality in all we do - taking active steps to reduce the avoidable differences in healthcare that some people face, working in partnership with communities.

Our strategy is underpinned by new values and we will work to ensure they are an everyday reality for all:

  • we are compassionate,
  • we are proud, 
  • we are inclusive, and 
  • we are one team 

This is an exciting moment as we look to the future with clarity on what we already do well and where we need to focus our energies to make an even bigger difference for the people we serve.

About the University Hospitals of Leicester NHS Trust:

http://www.leicestershospitals.nhs.uk/aboutus/work-for-us/current-vacancies/

 

Swydd-ddisgrifiad a phrif gyfrifoldebau manwl

Co-ordination of specified trials in accordance with study protocol and take responsibility for:

  • With supervision- study set up

  • Screening and recruitment of study participants

  • Organisation of any necessary study visits,  tests and investigations as detailed within the protocol.

  • Sample  retrieval, centrifuging, pipetting,  and  storage, liaising with the hospital and external laboratories when appropriate.

  • Resolving data queries raised by sponsoring organisations.

  • Archiving all study related material including patient’s notes after study closure.

  • Reporting and submitting of Serious Adverse Events (SAEs) from this site within stipulated timeframes to sponsor organisations and the Research and Innovation Office.

  • Tracking Serious Unexpected Event reporting

  • Maintaining and updating study specific site files.

  • Communicating with PI, clinical teams, research team and study sponsor. 

please see job description/person specification for further details on the role

Manyleb y person

Training and Quailifications

Meini prawf hanfodol
  • Registered Nurse on appropriate part of the register with current NMC Registration
  • Evidence of on-going professional development
Meini prawf dymunol
  • Evidence of specialist training or willingness to undertake additional specialist/academic training

Experience

Meini prawf hanfodol
  • Clinical skills including: ECG, Venepuncture
  • Knowledge of the clinical trial lifecycle, including experience of the set up and performance management of clinical research studies
  • Knowledge of good clinical practice and GDPR
Meini prawf dymunol
  • Experience in clinical specialty
  • Clinical research experience

Skills

Meini prawf hanfodol
  • Proven verbal communication skills with different staff groups
  • Attention to detail
  • Ability to problem solve
  • Ability to manage time effectively, prioritise work and to deliver results consistently to deadlines
  • Clinical skills including: ECG, IV drug administration and venipuncture
  • Good IT Skills, particularly in the use of Web applications and MS Office
Meini prawf dymunol
  • Trained in administration of intravenous therapies

Communication and relationship skills

Meini prawf hanfodol
  • Proven verbal communication skills with different staff groups Ability to educate and support colleagues, patients and carers

Analytical and Judgement skills

Meini prawf hanfodol
  • Basic understanding of research design and methodology
  • Awareness of current national systems and structures for the approval, management and monitoring of clinical research in the NHS
Meini prawf dymunol
  • Knowledge of the clinical trial lifecycle, including experience of the set up and performance management of clinical research studies

Bathodynnau ardystio / achredu cyflogwyr

Apprenticeships logoCare quality commission - Goodhttps://www.gov.uk/government/publications/kickstart-scheme-employer-resources/kickstart-scheme-brand-guidelinesMindful employer.  Being positive about mental health.Disability confident committedHappy to Talk Flexible Working

Gofynion ymgeisio

Rhaid i chi gael cofrestriad proffesiynol priodol yn y DU.

Mae'r swydd hon yn ddarostyngedig i Orchymyn Deddf Adsefydlu Troseddwyr 1974 (Eithriadau) 1975 (Diwygio) (Cymru a Lloegr) 2020 a bydd angen cyflwyno Datgeliad i'r Gwasanaeth Datgelu a Gwahardd.

Dogfennau i'w lawrlwytho

Gwneud cais ar-lein nawr

Rhagor o fanylion / cyswllt ar gyfer ymweliadau anffurfiol

Enw
Donna Alexander
Teitl y swydd
Senior Research Nurse
Cyfeiriad ebost
[email protected]
Rhif ffôn
0116 258 3839
Gwybodaeth i gefnogi eich cais

Judith Fisher  Senior Research Nurse

[email protected]  0116 250 2541

Gwneud cais ar-lein nawrAnfonwch hysbysiadau ataf am swyddi gwag tebyg