Junior Research Support Facilitator
| Dyddiad hysbysebu: | 17 Tachwedd 2025 |
|---|---|
| Cyflog: | £24,937.00 i £26,598.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £24937.00 - £26598.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 01 Rhagfyr 2025 |
| Lleoliad: | Derriford, Plymouth, PL6 5FP |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | C9216-25-1526 |
Crynodeb
Advice and Support To act as a first point of contact for researchers, receiving queries by telephone, e-mail and in personwith an ability to guide them clearly to the appropriate person for guidance through the complicatedR&D application processes. Researchers may be very experienced or may be attempting their firstforays into research - the ability to target and adapt communication style is therefore crucial. To become proficient in the use of our web-based electronic research database such as EDGE to enter,update and retrieve project information, to be able to use the web-based systems eg: NIHR operatingdata platform ODP . Liaise with and support investigators, research nurses, trial co-ordinators, Clinical Research NetworkStaff, and external Clinical Research Associates to ensure full trial documentation sets are availableand in place before authorisation of R&D Confirmation of Capacity and Capability. The completion ofapplications must be organised in a timely and efficient manner. Provide effective and timely communication with ethics committees, R&D offices, investigators and themulti-disciplinary teams, pharmaceutical companies and other research organisations such as theUniversities. R&D Approvals Facilitation Liaise with the R&D Finance team to ensure that Clinical Trials Agreements are in place and the studiesare fully costed before approval is given. Making the R&D Finance team aware of any potential studydelays. To learn to identify the different types of R&D projects (Clinical Trial of an Investigational MedicinalProduct [CTIMPs] and non-CTIMPs, device studies, genetics, Phase I, commercial and academic), inorder to make appropriate and accurate judgements concerning their approval and governancerequirements. To be aware of and deliver studies to national and local targets and timelines, whilst also being sensitiveto the wider research environment and understanding the possible impact on a delivery teams othercommitments to research. To learn to complete the necessary governance checks and administration tasks of studies such ascontract type and Statement of Events (SoE). To ensure that all local and study wide checks are up todate, reflecting information in the R&D study files, in a timely and accurate manner and to be aware ofthe implications of inaccuracy. Appropriately identify when external researchers may require Research Passports, Honorary Contractsor Letters of Access for studies and to notify the line manager accordingly, in order to issue thedocuments in a timely fashion. Work closely with integrated teams within the R&D Office and teams across the South West Peninsulain collation of full document sets. To set up and maintain R&D study files in accordance with the latest Trust Standard OperatingProcedures (SOPs), International Conference on the Harmonisation of Good Clinical Practice (ICHGCP) and other regulatory body requirements. To draft and issue appropriately signed Trust Approval Letters/emails, containing accurate informationand to disseminate copies to all relevant parties in a timely and professional manner. For further details please see the attached JD & PS