Clinical Trial Coordinator - Chelsea, United Kingdom - The Royal Marsden NHS Foundation Trust
Description
Applications are invited for a Clinical Trial Coordinator. This is a 12 month fixed-term post, with possibility of extension.
The Royal Marsden NHS Foundation Trust has an international reputation for high quality patient care, education and research and its partnership with The Institute of Cancer Research (ICR) has created the largest comprehensive cancer centre in Europe.
This role is based within the Lung Research Team at The Royal Marsden (located at two sites - Sutton, Surrey and Chelsea, London), which is world renowned for excellence in clinical care and clinical research.
For further details contact:
- Responsibility for the day to day coordination and oversight of specific hosted and some sponsored clinical trials in the Department.
- Lead on the setup of specific clinical trials in accordance with regulatory, sponsor and organisational requirements.
- To be an active member of the department, providing regular reports on activity within the Department and highlighting areas of concern.
Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer.
We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services.
We have two hospitals - one in Chelsea, London, and one in Sutton, Surrey - as well as a Medical Daycare Unit in Kingston Hospital.
At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.At the heart of the hospital is our dedicated team.
We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways.
There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance.
We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements.
For further information on this role, please see the attached detailed Job Description and Person Specification:- Initiate and manage day to day running of allocated trial(s) in accordance with Good Clinical Practice (GCP) and The Royal Marsden (RM) / Institute of Cancer Research (ICR) Standard Operating Procedures (SOPs)
- To ensure trials do not commence until all regulatory, sponsor and local R&D requirements are satisfied
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