Job description
The post will be based within the Academic Department of Paediatrics, University of Cambridge, and the Neonatal Unit at Cambridge University Hospitals NHS Foundation Trust.
The primary role of the post holder is to provide clinical input into the design and delivery of key clinical studies evaluating the efficacy, safety and usability of novel glucose monitoring devices in newborn infants. The Fellow will support the multidisciplinary research team to deliver the groups portfolio of studies in accordance with Good Clinical Practice (GCP), including single-centre physiological studies, device trials, and larger CTIMP studies.
This post is designed to develop skills in clinical research methodology, trial management and academic writing, and offers excellent opportunities for a motivated individual to develop their own area of interest and to prepare applications for further research funding or higher degrees.
The ideal post holder will have a sound knowledge of glucose monitoring technology and an understanding of protocol design and ethical applications. They will be enthusiastic about working collaboratively alongside others in the research team including PhD and post-doctoral research associates and research nurses.
The timetable will be dependent on the evolving study, education demands of the individual, and the department. An essential part of the role is flexibility to be available to support the recruitment and delivery of clinical studies. There is no clinical commitment to the post, however there are often opportunities to undertake locum clinical shifts within NICU for those wishing to maintain their clinical skills.
Please refer to the Job description and Person specification attached for further details on the main responsibilities and duties for this post.
Job description
Job responsibilities
The post will be based within the Academic Department of Paediatrics, University of Cambridge, and the Neonatal Unit at Cambridge University Hospitals NHS Foundation Trust.
The primary role of the post holder is to provide clinical input into the design and delivery of key clinical studies evaluating the efficacy, safety and usability of novel glucose monitoring devices in newborn infants. The Fellow will support the multidisciplinary research team to deliver the groups portfolio of studies in accordance with Good Clinical Practice (GCP), including single-centre physiological studies, device trials, and larger CTIMP studies.
This post is designed to develop skills in clinical research methodology, trial management and academic writing, and offers excellent opportunities for a motivated individual to develop their own area of interest and to prepare applications for further research funding or higher degrees.
The ideal post holder will have a sound knowledge of glucose monitoring technology and an understanding of protocol design and ethical applications. They will be enthusiastic about working collaboratively alongside others in the research team including PhD and post-doctoral research associates and research nurses.
The timetable will be dependent on the evolving study, education demands of the individual, and the department. An essential part of the role is flexibility to be available to support the recruitment and delivery of clinical studies. There is no clinical commitment to the post, however there are often opportunities to undertake locum clinical shifts within NICU for those wishing to maintain their clinical skills.
Please refer to the Job description and Person specification attached for further details on the main responsibilities and duties for this post.