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Clinical Trial Manager
salary: Grade 7: £36,024-£40,521 per annum
organization part: Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS)
application opening date: 2024-03-28T09:00:00+00:00
notation: 169793
comment: We are looking for a Clinical Trial Manager to join the Experimental Medicine and Rheumatology (EMR) trials groups within the UKCRC accredited Oxford Clinical Trials Research Unit (OCTRU) based in the Botnar Research Centre, Headington, Oxford. Following a successful funding application to the NIHR, the Experimental Medicine and Rheumatology (EMR) trials group are seeking a Clinical Trial Manager to take day to day responsibility for the management of clinical trials within their portfolio. The EMR trials group manages a wide variety of trials, in a variety of conditions spanning rheumatology and musculoskeletal conditions, experimental medicine and COVID-19, from set up to archiving. All trials are run as part of the UKCRC registered Oxford Clinical Trials Research Unit (OCTRU), which is one of the largest CTUs in the UK. You will be a key member of our friendly team ensuring the trial is efficiently planned and runs to time and target and in compliance with the relevant regulations and OCTRU SOPs. You will assist in finalising the protocol and other documents required for trial wide approvals; prepare and update trial documentation such as training material for collaborating sites, trial manuals and trial specific instructions as well as input to other key trials documents, including progress and final reports, and publications. You will work to design case report forms and associated documentation in collaboration with the trial statistician and Chief Investigator then work with the trial programmer to facilitate the set-up and testing of the trial database systems for randomisation, data capture and report generation. The post holder may also line manage junior staff members. You will be educated to degree level in a biomedical or associated subject with familiarity of UK clinical research structures, regulatory and ethical systems. You will have proven experience of the day-to-day management of clinical trials, to a high standard of Good Clinical Practice. Prov…
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based near: Botnar Research Centre
application closing date: 2024-04-16T12:00:00+01:00
formal organization: University of Oxford
contact: HR team, NDORMS
further particulars: 169793 JD Final.pdf
subject: research
type: Vacancy
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value: Job Description _________________________________________________________________________ Summary Job title Clinical Trial Manager Division Medical Sciences Division Department Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences Location Botnar Research Centre, Windmill Road, Oxford, OX3 7LD Grade and salary Grade 7: £36,024-£40,521 per annum Hours Full time (Part time 0.8 FTE over min 4 days considered) Contract type Fixed term until (31 August 2027) Reporting to Clinical Trials Operational Lead – Experimental Medicine and Rheumatology / Senior Clinical Research Manager, with accountability to Chief Investigator and grant holder Vacancy reference 169793 Additional information A lower grade offer may be made (Grade 6: £32,332 - £38,205 p.a.) with commensurate reduction in responsibilities (and amendment in job title to Trainee Clinical Trial Manager if a suitable candidate cannot be found to fill the Grade 7 position. The role Following a successful funding application to the NIHR, the Experimental Medicine and Rheumatology (EMR) trials group are seeking a Clinical Trial Manager to take day to day responsibility for the management of one or more clinical trials within their portfolio. The EMR trials groups manages a wide variety of trials, from set up to archiving, in a variety of conditions spanning rheumatology and musculoskeletal conditions, experimental medicine and COVID-19. All trials are run as part of the UKCRC registered Oxford Clinical Trials Research Unit (OCTRU). Your primary role will be to efficiently develop and coordinate the multi-centre trial on a day-to-day basis in compliance with OCTRU’s Standard Operating Procedures and Good Clinical Practice (GCP), ensuring study milestone through to preparation for archive are met including timely data collection. You will work closely with the Chief Investigator and other stakeholder to achieve this and be responsible for keeping stakeholders up to date with progress. The post hold…

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