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and codes of practice pertaining to the conduct of clinical trials Able to learn and work to SOPs Strong planning and organisational skills including the ability to prioritise, manage multiple tasks and
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Significant experience of monitoring multi-centre clinical trials in accordance with GCP (including source data verification) Working knowledge of the regulations, guidance and codes of practice pertaining
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and code through proactive thinking and vigorous testing, as well as iterative improvement Optimise Moodle performance, accessibility, and front-end behaviours. Engage with open-source development
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