The post holder will assist with participant identification and recruitment, obtaining informed consent from patients and will have responsibility for organising participant visits, collection and processing of participant samples, completion of case report forms and maintenance of study documentation according to Good Clinical Practice (ICH -GCP). You will have experience working in the UEC and Medicine Division and ideally be familiar with their systems. Clinical research experience within the NHS is desirable but full training and mentoring will be provided.
Responsibilities include:
1. Assisting with participant identification and recruitment
2. Obtaining informed consent from patients
3. Organising participant visits
4. Collecting and processing participant samples
5. Completing case report forms
6. Maintaining study documentation according to Good Clinical Practice (ICH -GCP)
Please see attached Job Description and Person Specification for further details.
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