# Critical Care Research Dietitian > NHS job listing from Job Clerk for Barts Health NHS Trust. ## Canonical URLs - **HTML:** https://www.jobclerk.com/job/critical-care-research-dietitian/f8b4b616-cdfc-4d1a-bfc8-27df21e5f06c - **Markdown:** https://www.jobclerk.com/job/critical-care-research-dietitian/f8b4b616-cdfc-4d1a-bfc8-27df21e5f06c.md ## Summary - **Status:** Live - **Employer:** Barts Health NHS Trust - **Town:** London - **Region:** London - **Country:** England - **Profession:** Dietitian - **Grade:** Band 7 - **Salary:** £58,133 - £65,261 per annum inc - **Contract type:** 12 months (Fixed term: 12 months) - **Employment type:** Full time, Flexible working, 37.5 hours per week - **Closing date:** 2026-06-15T23:59:00.000Z - **Posted:** 2026-06-02T08:42:48.970Z - **Source information URL:** https://www.healthjobsuk.com/job/UK/London/London/Barts_Health_NHS_Trust/NIHR_Puthucheary/NIHR_Puthucheary-v8049498 - **Application URL:** https://apps.trac.jobs/job-advert/8049498?ShowJobAdvert=&feedid=9002 - **Employer website:** https://www.bartshealth.nhs.uk ## Job Content ### Job overview This is an exciting opportunity to work in the world-leading Critical Care & Perioperative Medicine Research Group (CCMPG) based jointly at Barts Health NHS Trust and Queen Mary University of London. This unique post combines clinical research activity with the opportunity to further develop leadership and research skills. The successful applicant will play a key role in a diverse multi-professional team of nurses, doctors, allied health professionals and specialist researchers. This role is appointable for one year in the first instance, extendable to 36 months. Informal discussions and visits are welcomed, please contact Carys Davies (\[email protected\]). ### Main duties of the job They will be responsible for the recruitment and data capture of anthropometric and physical function data for the ASICS II trial across the London trial sites and working with the research team on day-to-day management of the ASICS trial programme of work. They will also be responsible for site education on trial feeding protocols and troubleshooting. They will ensure all projects are run according to Regulatory requirements, guidelines, GCP and to the study protocol.  They will liaise frequently with trial chief/principal investigators and the clinicians responsible for patient care. Further responsibilities may be allocated depending on the specific skills that the applicants have and/or wish to develop. ### Detailed job description and main responsibilities We are dedicated to being an outstanding place to work and will work with you to get the best experience. We know flexible working is not a one size fits all and will mean something different to everyone. We are inclusive, so if you are interested in flexible working, please speak to the recruiting manager. The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience, and knowledge required. For both documents, please view the attachment/s below. ## Job Details This is an exciting opportunity to work in the world-leading Critical Care & Perioperative Medicine Research Group (CCMPG) based jointly at Barts Health NHS Trust and Queen Mary University of London. This unique post combines clinical research activity with the opportunity to further develop leadership and research skills. The successful applicant will play a key role in a diverse multi-professional team of nurses, doctors, allied health professionals and specialist researchers. This role is appointable for one year in the first instance, extendable to 36 months. Informal discussions and visits are welcomed, please contact Carys Davies (\[email protected\]). ## Job Description They will be responsible for the recruitment and data capture of anthropometric and physical function data for the ASICS II trial across the London trial sites and working with the research team on day-to-day management of the ASICS trial programme of work. They will also be responsible for site education on trial feeding protocols and troubleshooting. They will ensure all projects are run according to Regulatory requirements, guidelines, GCP and to the study protocol. They will liaise frequently with trial chief/principal investigators and the clinicians responsible for patient care. Further responsibilities may be allocated depending on the specific skills that the applicants have and/or wish to develop. ## Responsibilities We are dedicated to being an outstanding place to work and will work with you to get the best experience. We know flexible working is not a one size fits all and will mean something different to everyone. We are inclusive, so if you are interested in flexible working, please speak to the recruiting manager. The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience, and knowledge required. For both documents, please view the attachment/s below. ## Person Specification ### Other **Essential** - Work and travel between all Bart’s Health NHS Trust sites - Ability to travel across all Greater London trial sites - Sufficient to perform the duties of the post with any aids and adaptations - Evidence of research based practice - Precise and methodical in working practice - Able to work under own initiative - Prepared to develop responsibilities and extend your role - Able to accommodate the demands of the post with flexible working as required - Proactive and self-motivated with ability to lead, motivate and empower others. - Ability to prioritise, meet tight deadlines and work independently on a number of projects. - Ability to work in a multi-professional arena - Ability to lead and manage meetings effectively. - Demonstrable effective team management ### Skills **Essential** - Interest in research and Service innovation - Computer Literate – Word Excel, PowerPoint, Outlook Access, SPSS - Demonstration of team working and interpersonal skills - Knowledge of current professional issues - Ability to work with all disciplines - Good organisational skills - Ability to problem solve and think critically - Good presentation skills **Desirable** - Understanding of ‘Good Clinical Practice’ for Clinical Research ### Knowledge **Essential** - Good Clinical Practice ### Experience **Essential** - Significant clinical experience - Experience within the intensive care and perioperative environment - Experience of working on quality improvement projects or clinical trials **Desirable** - To have contributed to written research papers or conference presentations - Published in an academic journal - Experience in critical care survivorship clinical work ### Qualifications **Essential** - BSc Nutrition & Dietetics or relevant postgraduate qualification - Post Graduate Diploma/equivalent experience - HCPC Registration **Desirable** - Good Clinical Practice Training ## Documents - [job description (pdf, 331.1kb)](https://www.healthjobsuk.com/documents?vdoc=10338871) - [our values and behaviours (pdf, 334.9kb)](https://www.healthjobsuk.com/documents?edoc=1119) - [candidate information pack (pdf, 549.5kb)](https://www.healthjobsuk.com/documents?edoc=2446) - [policy statement on the recruitment of ex-offenders (pdf, 92.0kb)](https://www.healthjobsuk.com/documents?edoc=1120) ## Agent Notes - This Markdown page is generated from the same Job Clerk job record as the HTML job detail page. - Use the canonical HTML URL for user-facing references. - Use the application URL when the user wants to apply on the source NHS site.