Clinical Trials Practitioner (UOH-TA-0371)
University of Hull
At University of Hull, we know diversity fosters creativity and innovation, and we want our community to represent the diversity of the world’s talent. We are committed to equality of opportunity, to being fair and inclusive, and to being a place where we all belong. We therefore particularly encourage applications from candidates who are likely to be underrepresented in University of Hull workplace.These include people from global majority backgrounds; people who have a declared disability; LGBTQI+ people; and women particularly for our Grade 9 and 10 roles.We reserve the right to close the advert early if a satisfactory amount of applications are receivedThe post holder will work within the purpose built clinical trials unit within Academic Diabetes, Endocrinology and Metabolism based in the new Allam Diabetes Centre at Hull Royal infirmary and to help make a positive impact to people living within the region.The Clinical Trials Practitioner will support a varied portfolio of clinical and applied health studies as well as pilot courses of diet and lifestyle invitations.The post holder will work closely with communities to increase representation across our portfolio of work, specifically in the field of obesity and its associated co morbidities.The post holder will be responsible for identification and recruitment of suitable candidates to participate in clinical trials specifically individuals living with obesity and overweight. 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.Specific Duties and Responsibilities of the postThe 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 in some areas, e.g. 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.Overall Purpose of the Role
For more information please see attached Job Description or for informal enquires please contact Zoe Hardey – Z.hardey@hull.ac.ukFurther details:Please note that we are unable to respond to enquiries, accept CVs or applications from Recruitment Agencies.
£27979 – 30487 per year
Kingston upon Hull
Sat, 10 May 2025 23:05:14 GMT
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