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Mae'r hysbyseb swydd hon wedi dod i ben ac mae'r ceisiadau wedi cau.
Clinical Trial Administrator
| Dyddiad hysbysebu: | 05 Tachwedd 2024 |
|---|---|
| Cyflog: | £31,944.00 i £34,937.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £31944.00 - £34937.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 19 Tachwedd 2024 |
| Lleoliad: | Chelsea, SW3 6JJ |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | C9282-24-1046 |
Crynodeb
For further information please refer to job description and personal specifications : Data Management Data Entry - Transcribing data from paper source document worksheets/ paper CRFs (case report forms) and entering them electronically into a database as part of EDC (electronic data capture). Data Queries - Data entered electronically are reviewed by monitors and may raise queries about certain inputs the Clinical Trial Administrator will need to respond to these queries, either by re-reviewing source documents to look for any typos or discrepancies, or by liaising with the clinical team for further information. Database Training - Being trained and using various databases and systems, with the ability to adapt between platforms with ease. Imaging requests and upload to submit electronic requests for anonymised imaging and imaging reports, and then upload them electronically onto web-based portals Navigating Digital Health Records being able to navigate the EPIC system (digital health records) to access patient records Maintaining trackers updating spreadsheets with information such as when patient visits have occurred Assisting Monitoring Visits Arranging visits liaising with the trial monitor/CRA to schedule monitoring visits according to protocol schedule, as well as both of your availability. This includes requesting IT access for the monitor. Facilitating the visit greeting the monitor at Main Reception, and escorting them to the monitoring room, ensuring their IT access works and they have access to the patient and trial folders Monitoring report after the visit, a monitoring report will be sent to the research team with a list of findings. The CTA should close any open findings relating to data.