Clinical Trials Practitioner & Team LeaderUniversity

The post holder will lead a team of Clinical Trials Practitioners, this project widens research access by delivering studies directly into underserved communities, including social housing estates, rural areas and traveller sites, through a Mobile Research Unit, GP practices, community venues and other local settings. By removing barriers such as travel, cost and stigma, residents gain opportunities to participate in obesity and lifestyle intervention studies that are typically hospital-based, improving inclusion and engagement. Based between the purpose built clinical trials unit within Academic Diabetes, Endocrinology and Metabolism, Allam Diabetes Centre at Hull Royal infirmary and the NHS mobile research units across the Humber region to help make a positive impact to people living with overweight, obesity and associated diseases.

The post holder will lead practitioners delivering community-based approach widening research access by delivering studies directly into underserved communities, including social housing estates, rural areas and traveller sites, through the Mobile Research Unit, GP practices, community venues and other local settings.

The post holder will be responsible for engaging stakeholders, building on established community relationships, identification and recruitment of suitable candidates to participate in clinical trials and clinical trials awareness. Further responsibilities include the management and facilitation of the clinical trials, including clinical work and technician tasks ensuring data is correctly gathered and recorded under the guiding principles of GCP.

The post holder will line manage a small team of Clinical Research practitioners and oversee community engagement and outreach work. The post holder will plan and deliver own workload and delegate workload and tasks to others

The post holder will assist with a variety of clinical research projects and clinical trials, particularly in diabetes and endocrinology.  Implement protocol guided care in Research setting; Observe patient condition, record clinical observations, adverse events & reports to PI.  To have responsibility for research samples to trial protocols. To work within clinical trial protocols and to ICH/GCP standards.

Ability to work without supervision, e.g. engaging with the public and stakeholders in the community, dealing with telephone and personal enquiries from staff, patients and carers, answering queries where possible and ensuring appropriate personnel informed for further action to be taken.

The post holder will manage and resolve day-to-day issues related to the operation of the mobile research unit, including logistical challenges and the prioritisation of clinical trials. They will also respond promptly and effectively to queries from study sponsors.

The postholder will plan the timetabling of community based venues and the associated staffing. Liaising with stakeholders and community leaders to ensure resource is in the right place and used effectively

A full UK driving licence and willingness to drive the mobile research unit as required (reasonable adjustments will be considered for candidates with disabilities).

Please upload a CV and cover letter describing how you meet the person specification for this job in the Resume/CV section of the online application form. For more information regarding the specific duties for the role please view the job description here

Applications close at 00:01am of the closing date listed. We reserve the right to close this vacancy early if we receive sufficient applications. If you are interested in this role, please submit your application as early as possible.