Clinical Trial Co-ordinator

2 weeks ago

Chelsea, United Kingdom The Royal Marsden NHS Foundation Trust Full time

Band 5 Clinical Trial Co-ordinator (Chelsea/Sutton)
Early Detection and Diagnosis
(ED&D)
1.0 WTE (Full Time)
1 year Fixed Term Contract

The post holder should have previous research experience, experience in cancer research is desirable. To be educated to degree level or equivalent experience, you will work within the guidelines and policies for the conduct of clinical trials, ensuring high standards of practice in accordance with the principles of GCP.

The successful applicant should have a flexible approach to their duties and the ability to work both as part of the team as well as independently. In addition; excellent communication, administrative and IT skills and being supportive and open to new initiatives are particularly valued by the team.

What’s in it for you?
- Opportunities to develop your clinical and research skills.
- Continuous on-going learning with internal and external courses available.
- Flexible working arrangements available.
- Working as a highly valued member of the MDT.
- The clinical trial co-ordinator will be responsible for the management of data and tissue samples for early diagnosis and detection research sponsored and managed by The Royal Marsden.
- The clinical trial co-ordinator will also complete other routine tasks required for the effective running of the research portfolio as directed by the Senior Trial Manager and Research Operations Lead.
- The clinical trial co-ordinator will be responsible for ensuring data is complete and managed in line with the protocol, data management plan and regulations.

The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. 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
- Assist with the preparation of investigator site files (ISF) and ensure site teams are aware of their responsibilities for the maintenance of the ISF at their site.
- Liaise with staff at research sites to provide information and documentation and support the set-up, implementation of amendments and running of the trial at each site.
- Obtain training records, investigator CVs and other documentation from sites as required.
- Ensure delegation logs for sponsor team and team at each site are completed and updated on a regular basis.
- Complete and maintain checklists and trackers for the clinical trials.
- Check the completeness of eligibility criteria information entered for research participants.

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