Clinical Trials Coordinator - Oxford, United Kingdom - University of Oxford
Description
Under the guidance of senior staff, you will take overall responsibility for the day-to-day management of a cohort study, setting up and supporting the participating sites and arranging their ethical/R&D approvals and Trial Agreements.
You will assist in the writing of study protocols, materials, training packages, and instructions, and in the design of case report forms and trial database systems.
You will also provide support by preparing for and organising Management Group and Steering committee meetings, and preparing progress reports for funders, oversight and ethics committees, and other stakeholders.
You will track expenditure against the project budget and (assisted by a Data Entry Clerk) oversee data entry and quality in the trial database.
This post is offered full-time, although part time (minimum 80% FTE) would be considered. It is a fixed term appointment for two years.The closing date for this position is
12 noon on Friday 03 February 2023
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