The post holder will assist with participant identification and recruitment, obtaining informed consent from patients and will have responsibility for organising patient visits, collection and processing of patient samples, completion of case report forms and maintenance of study documentation according to Good Clinical Practice (ICH -GCP). You will have experience working in one of our Trust Divisions and ideally be familiar with their systems. Clinical research experience within the NHS is desirable but full training and mentoring will be provided.
Please see attached Job Description and Person Specification for further details.
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