Clinical Research Fellow Respiratory Medicine

We are an award winning organisation providing care at two main hospital sites-Chelsea and Westminster Hospital and West Middlesex University Hospital-and a number of community-based services across London, such as sexual health and HIV clinics.

With 6,700 members of staff, we are proud to care for a diverse population of one million people. We are committed to ensuring that our workforce is just as diverse with a strong mix of skills and abilities.

Our staff are at the very heart of our organisation and we recognise the valuable contribution that each and every person working at the Trust makes. One of our Trust priorities is to be an employer of choice-a place where people want to start their career and to grow with us through continued education, professional development and support .

Clinical Research Fellow Respiratory Medicine NHS Medical & Dental: Clinical Research Fellow

Main area Research Grade NHS Medical & Dental: Clinical Research Fellow Contract Fixed term: 12 months (12 months from start date) Hours Full time - 40 hours per week Job ref 289-CR-165

Site Chelsea & Westminster NHS FT Town London Salary £54,499 - £67,325 Per Annum Salary period Yearly Closing 20/08/:59

Job overview

The job is fixed term for 12 months with further scope of extension. The post holder will support and manage high quality clinical research in Respiratory Medicine, according to ICH good clinical practice guidelines. The post holder will work closely with Dr Dexter Wiseman and Clinical Investigators at Chelsea & Westminster Hospital and Professor Jadwiga Wedzicha's group at the National Heart & Lung Institute (50:50 split). At Chelsea & Westminster Hospital, the Clinical Research Fellow (CRF) will be involved in the development of protocol, guidelines and the post holder will ensure that governance arrangements are maintained throughout duration of studies; and studies are managed in accordance with study protocols, national and international legislation and guidance (e.g. Research Governance Framework, Clinical Trial Regulations, GCP); assessing patient suitability for studies, screening, obtaining informed consent; and recruiting patients in line with agreed targets, data collection and maintaining research study records.

Main duties of the job

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.