Research and Innovation Pharmacist
| Dyddiad hysbysebu: | 11 Mehefin 2025 |
|---|---|
| Cyflog: | £53,755.00 i £60,504.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £53755.00 - £60504.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 25 Mehefin 2025 |
| Lleoliad: | Ashton U Lyne, OL67SR |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | C9311-25-0471 |
Crynodeb
Develop, review and disseminate guidelines and SOPs for management of Clinical Trials of Investigational Medicinal Products (CTIMPS) Advise Principal Investigators (PIs) on the legislation and procedures for carrying out clinical trials within PCFT Support PIs with recruitment to studies involving the wider pharmacy team as appropriate Advise PIs and other researchers of the current regulations relating to clinical trials applications (Medicines for Human Use (Clinical Trial) Regulations 2004 and subsequent amendments) and provide detailed support with clinical trials applications as required. Assess the future implications for the Trust of trial outcomes and advise R&I and pharmacy staff of these implications as required. Be responsible for the review of clinical trial protocols and advise on the pharmaceutical aspects of trial conduct, in line with the European Directive. Ensure that all clinical trial medicine supplies comply with the National Standards of Good Manufacturing Practice (annex 13). Source clinical trial supplies according to National Standards as required for investigator-led trials. Provide a randomisation and blinding service where necessary. Assess the pharmaceutical service implications of all new clinical trials on the Trust, including wider supply and administration issues using the trust risk assessment tool. Be responsible for the management of all clinical trial dispensing within the Trust and in conjunction with acute Trust pharmacies via SLAs. Ensure the management of clinical trial documentation and storage in accordance with National Guidelines at local acute trust sites. Ensure the security of trial medication, randomisation codes and PIN numbers at all times in line with Good Clinical Practice and company SOPs. Develop a reputation as a source of specialist advice on clinical trials for healthcare professionals within the Trust and primary care. Be a lead in the PCFT OptiMed research unit further expanding the unit