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Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS)
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Clinical Trial Coordinator
formal organization: University of Oxford
type: Vacancy
comment: This role will contribute to the successful running of the growing portfolio of trials managed by the Experimental Medicine and Rheumatology (EMR) trials group within Oxford Clinical Trials Research Unit (OCTRU), based in the Botnar Research Centre, Headington, Oxford. Under the guidance of senior staff and/or trial manager , you will take responsibility for the coordination of areas of trial management such as site set up, site management, data management and site closure activities and will be the key point of contact for participating sites for these activities. You will also provide support by undertaking tasks such as central monitoring; drafting and submitting amendments; databases testing and management of user accounts. You will be expected to work independently with minimal supervision across a number of trials within the group and to provide cover for periods of absence of Trial Manager(s). You may line manage and/or provide training for junior trial staff. You will be educated to at least A-Level standard or hold equivalent qualifications/experience and have previous experience in trial coordination, administration or support role. You will have knowledge of UK clinical research structures, regulatory and ethical systems, and experience of working to a high standard of Good Clinical Practice. Effective organisational skills including the ability to prioritise workload, be adaptable to changing priorities, a critical and intelligent attention to detail and high standards of accuracy is also essential. Experience of data management relating to research participants is desirable. This post is offered full-time, although part time (minimum of 60% FTE) would be considered. It is a fixed term appointment for 12 months. A mixture of office and remote working can be agreed. The closing date for this position is 12 noon on 11/10/2023 Interviews are expected to take place on Wednesday 18th October 2023. You will be required to upload a CV and supporting statement a…
based near: Botnar Research Centre
further particulars: 168436_JD
organization part: Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS)
application closing date: 2023-10-11T12:00:00+01:00
contact: HR Team, NDORMS
application opening date: 2023-09-27T09:00:00+01:00
spatial: Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, Windmill Road, Oxford, OX3 7LD
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value: Job Description _________________________________________________________________________ Summary Job title Clinical Trial Coordinator 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 6: £32,332-£38,205 per annum Hours Contract type Full time Fixed-term (12 months) Reporting to Clinical Trials Operational Lead – Experimental Medicine and Rheumatology Vacancy reference 168436 The role This role will contribute to the successful running of the growing portfolio of trials managed by the Experimental Medicine and Rheumatology (EMR) trial group within Oxford Clinical Trials Research Unit (OCTRU). Under the guidance of the trial manager and/or senior staff, the post holder will take responsibility for the coordination of areas of trial management such as site set up, site management data management and site closure activities. The post holder will utilise their clinical trials experience and knowledge to provide administrative and technical support to EMR trial group. The post holder will be expected to work independently with minimal supervision across a number of trials within the group. The post holder will provide cover for periods of absence of the Trial Manager and may line manage junior trial staff. Responsibilities 1. Take responsibility for the coordination of specific areas of trial management such as site set up, site management, data collection, site closure. 2. Provide updates and report issues or concerns to the Trial Manager and/or senior staff. Use initiative to tackle any practical difficulties encountered under their guidance. 3. Contribute to the production and updating of trial documents such as ISF documents, training material for sites and trial specific instructions, and contribute to the maintenance of the TMF. 4. Provide support to Trial Managers by undertaking tasks such as central moni…

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