Senior Research Sister / Charge Nurse
| Dyddiad hysbysebu: | 15 Awst 2025 |
|---|---|
| Cyflog: | £47,810.00 i £54,710.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £47810.00 - £54710.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 29 Awst 2025 |
| Lleoliad: | Coventry, CV2 2DX |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | C9218-25-0896 |
Crynodeb
Work autonomously to manage a caseload of patients acting as a professional to ensure care to patients is delivered according to Trust policies and procedures and the research protocol delivery high standards and continuity of clinical care for study participants. Maintain strong relationships and communication channels with other key personnel such as multidisciplinary teams, clinical wards areas. Attend Multi-disciplinary Meetings, and appropriate clinics, to assess volunteers/patients for eligibility for research and recruit new patients, to act as a resource to the members of the MDT. Ensure that trial specific clinical investigations / procedures are undertaken as required by the research protocol in order to establish eligibility and maintain safety in the trial by all team members. Take relevant samples as required by the study protocol such as blood samples, package and dispatch as defined. Ensure safe and appropriate storage of specimens in accordance with trial protocols and regulatory / Trust guidance. Ensure all team members undertake relevant training and assessment of competence, working within scope of professional practice prior to undertaking any clinical procedures / administration of treatments associated with the research treatment regimes. Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial by all team members. Ensure staff monitor treatment toxicity/side effects reporting to the relevant personnel, recording as required assisting in any required changes to treatment as required by the protocol Ensure all staff record and report adverse /serious adverse events as classified in the study protocol criteria which occur whilst patient is in the clinical trial e.g. hospital admission since last study visit Ensure accurate documentation of patients events in nursing/medical notes and study specific case report forms. Provide ongoing information, education and support to patients (and their significant others) regarding clinical trials and their care. For further details please see the attached job description.