ENHT is seeking to maintain and expand the Mount Vernon Cancer Centre staff as we move to an exciting new future.
We welcome applications from those who would relish the opportunity to be part of new and developing cancer service, building on the excellent reputation, research and patient experience the Cancer Centre already delivers.
In addition, you will receive a High Cost Area Supplement of 15% of your basic salary, subject to a minimum payment of £4,1and a maximum payment of £5,177per annum pro rata.
Please see the attached Job Description and Person Specification information pack for further detailed information regarding this role.
We are recruiting for a Senior Clinical Trials Coordinator who shares our vision to be trusted to provide consistently outstanding care and exemplary service to our patients.
We are looking for an enthusiastic and energetic individual with a clear understanding of issues relating to management of clinical research in the NHS.Previous experience would be beneficial but not essential as training will be provided.
You will be joining our Clinical Oncology Research Teams who sees research as an essential part of everyday activity and has just successfully implemented a research strategy to enhance patient experience and outcomes through research and innovation.
You will receive a High Cost Area Supplement of 15% of your basic salary, subject to a minimum payment of £4,314 and a maximum payment of £5,436 per annum pro rata.
Our Values are Include, Respect and Improve. It is important that you understand and refer to our values during your recruitment process and beyond!
The main purpose of the role is to support the clinical research team with all aspects of clinical trials administration, according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and trust policies.
You will provide support to the Research Nurses and wider Clinical Research Team and undertake supervision of Band 4 Clinical Trial Coordinator(s) when required.
Assist with monitoring administration of research grants or charitable grants and confirming that appropriate payments are made, including remuneration of staff, by liaising with R&D Finance Department.
Oversee the efficient and timely set up of clinical trials and workforce planning on a daily basis to meet organisational requirements and oversee and maintain databases/ spreadsheets and produce monthly progress reports on recruitment.
You will manage own workload for daily trial activity including case report form completion and amendment processing to meet internal and external deadlines.
ENHT is seeking to maintain and expand the Mount Vernon Cancer Centre staff as we move to an exciting new future.
We welcome applications from those who would relish the opportunity to be part of new and developing cancer service, building on the excellent reputation, research and patient experience the Cancer Centre already delivers.
In addition, you will receive a High Cost Area Supplement of 15% of your basic salary, subject to a minimum payment of £4,1and a maximum payment of £5,177per annum pro rata.
Please see the attached Job Description and Person Specification information pack for further detailed information regarding this role.
We are recruiting for a Senior Clinical Trials Coordinator who shares our vision to be trusted to provide consistently outstanding care and exemplary service to our patients.
We are looking for an enthusiastic and energetic individual with a clear understanding of issues relating to management of clinical research in the NHS.Previous experience would be beneficial but not essential as training will be provided.
You will be joining our Clinical Oncology Research Teams who sees research as an essential part of everyday activity and has just successfully implemented a research strategy to enhance patient experience and outcomes through research and innovation.
You will receive a High Cost Area Supplement of 15% of your basic salary, subject to a minimum payment of £4,314 and a maximum payment of £5,436 per annum pro rata.
Our Values are Include, Respect and Improve. It is important that you understand and refer to our values during your recruitment process and beyond!
The main purpose of the role is to support the clinical research team with all aspects of clinical trials administration, according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and trust policies.
You will provide support to the Research Nurses and wider Clinical Research Team and undertake supervision of Band 4 Clinical Trial Coordinator(s) when required.
Assist with monitoring administration of research grants or charitable grants and confirming that appropriate payments are made, including remuneration of staff, by liaising with R&D Finance Department.
Oversee the efficient and timely set up of clinical trials and workforce planning on a daily basis to meet organisational requirements and oversee and maintain databases/ spreadsheets and produce monthly progress reports on recruitment.
You will manage own workload for daily trial activity including case report form completion and amendment processing to meet internal and external deadlines.