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Clinical Trials Assistant | Hull University Teaching Hospitals NHS Trust
| Posting date: | 01 August 2024 |
|---|---|
| Salary: | Not specified |
| Additional salary information: | £22,816 - £24,336 Per annum |
| Hours: | Full time |
| Closing date: | 31 August 2024 |
| Location: | Hull, HU3 2JZ |
| Company: | Hull and East Yorkshire Hospitals NHS Trust |
| Job type: | Permanent |
| Job reference: | 6458640/356-24-6458640 |
Summary
The Diabetes Endocrinology and Metabolism Trials Teams based at In the Allam Diabetes Centre, Hull Royal Infirmary are looking for a Clinical Trials Assistant to work within the unit to support an increasing portfolio of clinical trials.
We are seeking an enthusiastic and motivated individual who will be responsible for assisting the clinical research team with all aspects of administration and delivery of protocol guided care relating to clinical trials according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and trust policies.
Experience of working in clinical research would be advantageous but not essential. It is however essential that applicants have a minimum of two years' experience of working with patients in a health care environment and either hold or be willing to work towards a level 3 qualification in a related field. The post-holder will be required to work with all members of the multi-disciplinary team in the recruitment, screening and care of patients in Diabetes Endocrinology and Metabolism clinical trials. The post requires excellent communication skills, an ability to prioritise workload and to work independently, unsupervised and flexibly.
Please note that this advertised vacancy does not meet the UKVI eligibility requirements for a Skilled Worker Visa and therefore HUTH would not be able to issue a Certificate of Sponsorship for this role.
The successful applicant will need to be enthusiastic and ready to work actively in supporting the established teams of Clinical Academics, Research Fellows, Research Practitioners and Trials coordinators in recruiting and following up patients who are participating in research trials. Liaison with external research partners such as pharmaceutical companies, research networks and clinical trials units will also be required.
Although the post holder's primary base would be The Diabetes Endocrinology and Metabolism Trials Unit, there is an expectation that the post holder will be flexible and responsive to the research needs of the organisation and may therefore be required to work in other research areas.
The Humber Health Partnership is one of the largest acute and community Partnership arrangements in the NHS, seeing well over one million patients every year and managing a budget of over £1.3 billion.
Made up of two Trusts - Northern Lincolnshire and Goole NHS Foundation Trust (NLAG) and Hull University Teaching Hospitals NHS Trust (HUTH) - our Partnership has significant ambitions and is committed to delivering world-class hospital and community services for the 1.65 million people we serve.
Together we employ nearly 20,000 staff. Our five main hospital sites are Diana, Princess of Wales Hospital, Scunthorpe General Hospital and Goole and District Hospital, for NLAG and Hull Royal Infirmary and Castle Hill Hospital for HUTH.
As Teaching Hospitals working with the Hull York Medical School, we both lead and contribute to research in many areas - biomedical research, primary care, palliative medicine, cardiovascular and respiratory medicine, vascular surgery, cancer surgery and oncology.
We believe that by developing a diverse, inclusive, innovative, skilled and caring workforce, we can deliver excellent care to our patients and a great future for our employees, our Partnership and our community.
Assist the research team including Principle Investigators and sub Investigators in the identification, recruitment and management of patients enrolled in a portfolio of NIHR commercial and non-commercial clinical trials.
Undertake procedures under the supervision of the medical team, having been trained, assessed and deemed competent in these activities.
Perform data-gathering, specified clinical tasks and administrative support for clinical research studies and research team.
To coordinate and input clinical trials data ensuring data is up to date and ensuring the completeness, accuracy and consistency of trial data in order to meet standards expected of sponsors and regulatory authorities
This advert closes on Thursday 15 Aug 2024