Clinical Research Fellow Respiratory Medicine
| Dyddiad hysbysebu: | 01 Gorffennaf 2025 |
|---|---|
| Cyflog: | £49,909.00 i £61,825.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £49909.00 - £61825.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 07 Gorffennaf 2025 |
| Lleoliad: | London, SW10 9NH |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | C9289-CR-22-A |
Crynodeb
Research Responsibilities a) To contribute to study protocol design in collaboration with Clinical Research Lead and Pharmaceutical Companies and Academic Institutions representatives. This will include the writing of patient information leaflets, design of case report forms (CRFs) and source documents in line with the R&D standard operation procedures (SOPs). b) To ensure appropriate consent for research is obtained from the relevant patients c) To write concept sheets and full protocols or amend such documents which relate to the primary research carried out in respiratory medicine. d) Contribute to the promotion of Chelsea and Westminster Hospital Research and Development and the National Heart & Lung Institute and creating further funding opportunities. e) To represent the unit at meetings both locally and as required, at national and international locations; this includes Investigator meetings and Study Initiation meetings as well as attendance at Research Ethics Committee meetings. f) To undertake clinical responsibilities and research activities in Phase I-IV Research in Medicine. g) To provide clinical and professional supervision at Chelsea and Westminster Hospital NHS Foundation Trust, in collaboration with the Assistant Director of Research and Development to doctors and other staff (e.g. research nurses, research assistants etc.). h) To ensure that the dignity, right, safety, and wellbeing of all trail participants and give priority at all times i) To be available to work flexible hours as may be required by the design of particular clinical trial or the departments needs. j) To participate in the analysis and publication of research results. k) To maintain up-to-date knowledge of all applicable R&D SOPs and follow these in daily research activities. l) To assess of all Serious Adverse Events (SAE) to determine whether a suspected unexpected serious adverse reaction (SUSAR) has occurred and to ensure timely reporting in line with the current applicable regulatory requirements. m) To keep well organised, legible and accurate records. n) To meet with study monitors regularly to assist with clarification of data queries in order to maintain quality assurance o) To participate in audits or inspection of Trust sponsored clinical trials as well as external sponsored studies as required. p) To assist in both internal and external training requirements (general and study-specific) in liaison with Lead Nurse and other Clinicians. q) The post-holder will be required to build on existing close relations with colleagues as part of a multidisciplinary team. He/she will also be required to support quality improvement, research and management of the service. r) To assist and help supervise post-graduate students and visiting workers s) To undertake appropriate administration tasks t) Contribute to departmental management as required u) To undertake any necessary training and/or development v) Any other duties commensurate with the grade of the post as directed by the Principal Investigators w) The post holder will be expected to contribute to the intellectual activities of their host department and to keep up to date with scientific advances in the field