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Associate Clinical Research Practitioner | University Hospitals of Leicester NHS Trust
| Dyddiad hysbysebu: | 19 Awst 2024 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | £25,147 - £27,596 per annum, pro rata |
| Oriau: | Rhan Amser |
| Dyddiad cau: | 18 Medi 2024 |
| Lleoliad: | Leicester, LE3 9QP |
| Cwmni: | University Hospitals of Leicester |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | 6476450/358-6476450-ITA |
Crynodeb
We are seeking an experience clinical associate research practitioner to join Research and Innovation (R&I) department at University Hospitals of Leicester NHS Trust as an ITU clinical associate research practitioner at Glenfield hospital as part of the NIHR Biomedical Research Centre – Respiratory and infection Theme.
The post holder will work alongside Principle investigators and support current ITU research staff in delivering high quality research and ensuring the completeness, accuracy and consistency of the data in order to meet standards expected for reporting to regulatory bodies.
The individual will provide clinical support to patients in clinical trials; such as taking samples, performing tests and physical measurements in accordance with the clinical trial protocol, and Good Clinical Practice.
The post holder should be adaptable, flexible and show initiative. In addition they need to show good communication skills, be able to liaise with all levels of staff, demonstrate good organisational skills and attention to detail, have good time management skills and be flexible as the working hours may not be fixed.
The post-holder may be required to work in other research areas across UHL if service needs arise.
This post will predominantly be a Monday - Friday office hours however may need flexibility depending on the study requirements.
• Research Trial Set Up and Initiation
• Assist with the acquisition and distribution of relevant trial documentation/equipment.
• To establish trial site files for each trial in accordance with ICH-GCP
• Collection of patient data from medical notes and completion of case record forms (CRF’s) and to liaise with clinical trial coordinators, research nurses and investigators to ensure accurate data collection
• Facilitate the secure filing and storage of study documentation in accordance with ICH- GCP and Research Governance and conduct quality assurance of documentation
• Take responsibility for liaising with clinical trials units/study sponsors regarding data queries and for checking and resolving data queries
• To evaluate patient eligibility, in liaison with other appropriate health care professionals for clinical trial entry, involving coordination of pre study tests, obtaining results and arranging appropriate appointments as per clinical trial protocols
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/
Management and co-ordination of specified trials and take responsibility for:
· Organisation of any necessary tests and investigations as detailed within the protocol.
· Sample preparation (e.g. blood, urine, tissue and faecal samples): retrieval, centrifuging, pipetting, slide making and preparation for storage, liaising with the hospital and external laboratories when appropriate.
· Maintaining logs of stored samples and freezer temperatures.
· Maintaining adequate stock levels of sample kits.
· Organising the logistical aspects of diagnostic specimens, packaging, and shipment, including handling of dry ice.
· Organising and completing follow up assessments including toxicity, Quality of Life assessments and telephone assessments.
· 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.
· Notifying General Practitioners of their patient’s involvement in a clinical trial.
please see job description/person specification for further details on the role.
This advert closes on Sunday 1 Sep 2024