{"interviewQueryText":"What are some good interview questions in British English for the job description below?\n\n-------------------------------------------\n\nSenior Research Nurse with Royal Papworth Hospital NHS Foundation Trust in Cambridge Bio Medical Campus, Cambridge\n\n On this page you will find a Role Profile which provides information about the hospital and full details about the role. We recommend that you review this and refer to it as you complete your application. Please include how you will meet the Trust Values Compassion, Excellence and Collaboration. If you would like more information about the role or working at Royal Papworth Hospital, please get in touch with the contact for this role. An exciting opportunity to work as a Senior Research Nurse has arisen in the CCLI Research Team. We are a team of experienced and dedicated professionals collaborating with our talented multi-disciplinary clinical teams to deliver a wide range of innovative high quality research trials to inform the future care of our patients. The R & D team support a large and growing portfolio of studies across multiple specialities. We offer a friendly working environment and are interested in your career development with a range of training opportunities available to help you fulfil your potential. We are looking to appoint an experienced Research Nurse who is, enthusiastic, motivated, proactive and who will enjoy the challenge of delivering high quality research. You will be based at the new Heart Lung Research Institute (HLRI) and Royal Papworth Hospital on the Cambridge Biomedical Campus. Planned interview date: Tuesday 14th May 2024 As a key member of the Research Team, you will be responsible for the set up and coordination of multiple clinical trials. Your duties include recruiting and consenting suitable patients, coordinating data collection, arranging, and conducting assessments, follow up appointments, tests and investigations which are specified by the study protocol. You will ensure that specified milestones are achieved on time, that high quality data is collected and that the trial is being conducted according to the ethically approved protocol and ICH-GCP standards. The post holder will be responsible for a portfolio of commercial clinical trials including randomised, controlled trials and observational studies. "}