HLRI CRF Clinical Trial Co-ordinator
Cambridge Bio Medical Campus, United Kingdom
Royal Papworth Hospital NHS Foundation Trust
and demonstrate that high quality data is being collected and that the trial is being conducted according to the ethically approved protocol and ICH-GCP standards. They will also coordinate data collection and data entry and responding to everyday queries from research nursing team and study participants including coordination and … delivery of a comprehensive, high-quality service within the CRF in accordance with Trust Policies, R&D SOPs, Good Clinical Practice (GCP) and all other regulatory requirements. *To contribute to the implementation, monitoring, improving and management of the CRF's Operations, policies and SOP and support its … in touch with the contact for this role. Person Specification Qualifications Essential Science graduate or equivalent level of Knowledge and experience Desirable Recent ICH GCP Training Experience Essential Experience of working in a clinical research environment within NHS, University or pharmaceutical industry Experience of working with multi-disciplinary teams. more »
Employment Type: Fixed-Term
Salary: £28407.00 - £34581.00 a year
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