Job Description

Medical Oncology Gastro-intestinal & Lymphoma Unit

Full time - 37.5 hours per week over 5 days per week.

Salary Scale:

AfC6

Based:

Sutton (Royal Marsden NHS Foundation Trust)



A very exciting opportunity has arisen in the GI & Lymphoma Unit at the Royal Marsden Hospital for a lead Data Manager for all Royal Marsden sponsored, Investigator lead, Clinical trials. At least 1 years' experience working in Gastrointestinal Cancer and working on MACRO is essential.



This person will be experienced in development of clinical trial databases in MACRO, creating and annotating Case Report Forms (CRFs), specification of validation checks and the testing of each individual Electronic Data Capture (EDC) database.

The role will also be responsible for the creation and review of data management plans, CRF completion guidelines, guidance documents and templates making recommendations for change where appropriate.



For an informal discussion, please contact Claire Saffery 0208 642 6011 x4480 or e-mail claire.saffery@rmh.nhs.uk



We require a Clinical Data Manager to lead the Data Management for all Royal Marsden sponsored, Investigator Lead clinical trials running through the Gastro-intestinal & Lymphoma Research Unit, communicating proactively and effectively with study team members, providing updates on projects and ensuring data management milestones are met to ensure all trials open in a timely manner with data capture processes in place for the first patient to be recruited. This post will be based at the Royal Marsden Hospital, Surrey although flexibility will be

required to work in our London offices on occasion.



The experience and motivated post-holder will be exposed to a number of clinical trials, supporting the development of clinical trial databases in MACRO, creating and annotating Case Report Forms (CRFs), specification of validation checks and the testing of each individual Electronic Data Capture (EDC) database. The role will also be responsible for the creation and review of data management plans, CRF completion guidelines, guidance documents and templates making recommendations for change where appropriate.



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 more information please refer to the job description and person specification:



Serving as the primary unit contact for data management for RM sponsored trials running through the GI &Lymphoma Unit, communicating proactively and effectively with the Trial team, ensuring data management milestones are met.



Assisting with the development of CRFs, assisting the programmers to define the individual trial specific database in MACRO, specify validation checks and perform validation of each programme



Create and review data management plans, guidance documents and templates, making recommendations for change where appropriate, including changes to accommodate study protocol amendments.



Assist with the review of clinical trial data ensuring ongoing data cleaning is managed effectively and efficiently, highlighting any issues that may affect data quality to the Trial Manager.