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Quality Assurance Officer
| Dyddiad hysbysebu: | 03 Gorffennaf 2024 |
|---|---|
| Cyflog: | £25,147.00 i £27,596.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £25147.00 - £27596.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 17 Gorffennaf 2024 |
| Lleoliad: | Liverpool, L12 2AP |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | C9411-24-0356 |
Crynodeb
. To undertake audits in line with the CRD rolling audit program. To undertake monitoring of studies and trial documentation. To liaise with CRD research delivery staff and the wider trust, e.g. laboratory managers & Consultants, to ensure appropriate QA processes are implemented and adhered to. 2. To liaise with Research Governance Manager to review critical and major findings resulting from internal/external inspections and to produce and implement CAPA reports 3. To assist with the review and closure of CAPA reports 4. To provide oral and written reports on activities to the Research Governance manager in line with overall responsibilities. 5. To undertake relevant training. To perform any other duties required by Research Governance Manager Communication and Relationships Analytical and Judgemental skills Planning and Organisational skills Please see JD attached for full Job Description Physical Dexterity Keyboard skills Physical requirement for prolonged periods of concentration when cross referencing information and data Frequent need to carry cumbersome trial files from clinical areas and within the offices Policy and Service Development Requirement to keep up to date with policy developments pertaining to QA and support implementation where necessary e.g. ICH GCP To provide information regarding the performance of the CRF/CRD vs QA metrics across the portfolio Education and Training To act as a QA resource for CRD/CRF staff and others involved in research studies within the trust To maintain an awareness of current advances in QA clinical research To continue professional development and attend training and meetings as required. Attend regular updates and feedback to multi-disciplinary team on developments in regulatory guidelines pertaining to QA for clinical research Attend annual UKCRF conference if required Research and Development As a member of the multi-disciplinary team there will be involvement in the entire process of supporting clinical trials and other research studies. Other To understand and adhere to local Trust policies and procedures The post holder has responsibility for safety as outlined in the hospitals policy and Health and Safety Work Act 1974 To maintain confidentiality at all times