This is an exciting opportunity for a new Clinical Trial Coordinator to join our team and be instrumental in providing high quality trial management which will advance the outcomes of important questions that transform the lives of patients.
The successful candidate will be instrumental in the day to day management of clinical trials. This includes ethics and regulatory applications and amendments, site set up and training, presenting at meetings and producing progress reports as required. The successful candidate will assist with any other clerical duties such as minutes taking and preparation and distribution of materials to research sites.
This role plays a key part in ensuring the success of our trials.
The Clinical Trial Coordinator will also engage in designing and reviewing the trial database as well as gain a good understanding of data management with potential line management responsibility of data entry clerks.
For informal enquiries, please contact via email:
Kath Starr - [email protected]
Jaclyn Bailey - [email protected]
We will consider applications for employment on a part-time or other flexible working basis, even where a position is advertised as full-time, unless there are operational or other objective reasons why it is not possible to do so.
Full details of the duties and selection criteria for this role can be found in the vacancy advert on the University of Warwick's jobs pages. You will be routed to this when you click on the Apply button.
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