Clinical Trial Manager

Job description

About

he University of Oxford is a stimulating work environment, which enjoys an international reputation as a world-class centre of excellence. Our research plays a key role in tackling many global challenges, from reducing our carbon emissions to developing vaccines during a pandemic.

The Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS) is part of the Medical Sciences Division and is the largest European academic department in its field, running a globally competitive programme of research and teaching. The Kadoorie Institute of Trauma, Emergency and Critical Care brings together interdisciplinary research across trauma and rehabilitation, emergency care and critical care, with a focus on improving outcomes for patients with life-threatening illness and injury. The Institute integrates expertise across these closely connected specialties within a single research environment. Based at the John Radcliffe Hospital, the centre of urgent and emergency care in Oxford, the Institute supports more than 100 multidisciplinary researchers working across the breadth of trauma, emergency and critical care research. Its research spans the use of routinely collected healthcare data and early- and late-phase clinical trials, enabling discoveries to be translated into improvements in clinical practice and patient care.

What We Offer

As an employer, we genuinely care about our employees’ wellbeing and this is reflected in the range of benefits that we offer including:

• An excellent contributory pension scheme

• 38 days annual leave

• A comprehensive range of childcare services

• Family leave schemes

• Cycle loan scheme

• Discounted bus travel and Season Ticket travel loans

• Membership to a variety of social and sports clubs

• This role also offers the opportunity for hybrid working

About the Role

In this role, you will work autonomously as a Trial Manager, taking overall responsibility for the day-to-day management of multi-centre randomised clinical trials. You will assist in finalising the protocol, study materials, training packages for collaborating sites and trial manuals, and prepare trial specific instructions. You will work to design data collection forms and associated documentation as required in collaboration with the trial statistician and Chief Investigator – then work with the trial programmer to assist in the design and testing of the trial database systems for randomisation, data entry, validation and report generation. This post involves obtaining and maintaining overall and site-specific ethical and R&D approvals for all sites and ensure Clinical Trial Agreements are in place before the research commences as well as providing line management and training for administrative trial staff (e.g. trial administrators, data entry clerks).