Job summary
An exciting opportunity has arisen within the GI & Lymphoma Research Team to work as a Clinical Trials Administrator at the forefront of research into Gastro-intestinal Cancer and Lymphoma. You will be based in our Sutton offices but will be expected to support the unit across both locations of the Royal Marsden, including Chelsea, when required.
Ideally, familiarity with medical terminology and GCSE/A level education, 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.
This is a pivotal role supporting clinical research within this unit. Your main duties would include collecting and collating data for commercial and academic trials, organising and attending monitoring visits with trial sponsors together with administrative support to the research team. You will be part of a multidisciplinary team including experienced medical and nursing staff taking part in an exciting portfolio of clinical research studies in GI Cancer and Lymphoma
You should have a flexible approach to your duties and the ability to work both as part of the team as well as independently playing a key role in supporting the GI & Lymphoma Unit activity. In addition you will have excellent communication, administrative and IT skills and be supportive and open to new initiatives.
Appointment will be on a fixed term contract for one year initially.
Main duties of the job
o To support the clinical research team with study administration as required to ensure the efficient and successful delivery of clinical trials and other studies according to Good Clinical Practice (GCP), standard operating procedures (SOPs), trust policies and all applicable regulations and governance structures.o To ensure timely and accurate entry of data and relevant information into appropriate database systemso To work with the clinical team to ensure prompt resolution of data queries.o To provide support to the clinical research team in daily trials activity and assist in workload management.
About us
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.
Details
Date posted
18 February 2026
Pay scheme
Agenda for change
Band
Band 4
Salary
£32,199 to £34,876 a year per annum
Contract
Fixed term
Duration
12 months
Working pattern
Full-time
Reference number
282-CR1274
Job locations
The Royal Marsden Hospital
Sutton
SM2 5PT
Job description
Job responsibilities
To ensure that data collection and (electronic) case report form (CRF) completion is performed to the required standards of the current EU, UK and FDA legislation, Trust SOPs and Sponsor contractual obligations.
To design and implement tools and guidance for clinical trial data capture.
Liaise with external agencies (eg. Sponsor organisations, R&D Departments and Local Ethics Committees etc) on behalf of Research Nurses and / or the Senior Trial Co-ordinator where required.
Act as a point of contact for trial sponsors and to communicate directly with them regarding data queries, monitoring visits and other enquiries relevant to the trial and research team.
To ensure timely and accurate entry of data and relevant information into appropriate database systems.
Support research staff with preparations for sponsor and external audits/inspections.
Assist in the collation of adverse reaction reports arising from clinical trials and entering data with support of the research nurse.
Job description
Job responsibilities
To ensure that data collection and (electronic) case report form (CRF) completion is performed to the required standards of the current EU, UK and FDA legislation, Trust SOPs and Sponsor contractual obligations.
To design and implement tools and guidance for clinical trial data capture.
Liaise with external agencies (eg. Sponsor organisations, R&D Departments and Local Ethics Committees etc) on behalf of Research Nurses and / or the Senior Trial Co-ordinator where required.
Act as a point of contact for trial sponsors and to communicate directly with them regarding data queries, monitoring visits and other enquiries relevant to the trial and research team.
To ensure timely and accurate entry of data and relevant information into appropriate database systems.
Support research staff with preparations for sponsor and external audits/inspections.
Assist in the collation of adverse reaction reports arising from clinical trials and entering data with support of the research nurse.
Person Specification
Education/Qualifications
Desirable
* Knowledge of ICH/GCP guidelines
Education/Qualifications
Essential
* Educated to at least GCSE/A level (or equivalent)
Experience
Essential
* Experience in working with databases
Desirable
* Good understanding of medical terminology
* Previous experience of working in the NHS or equivalent
Skills/Abilities/Knowledge
Essential
* Excellent administrative and organisational skills
* Competence in research orientated PC software including Microsoft Office packages
* Excellent oral and written communication skills with the ability to work independently within a team environment
* Good attention to detail
* Good level of spoken and written English.
* Ability to grasp new concepts quickly and to have clear legible handwriting.
Desirable
* Understanding of clinical trials and regulations governing clinical research
* Experience of data entry and data management
Other Requirements
Essential
* Able to work on both sites and to be flexible to meet the needs of the role
Desirable
* Willingness to travel within UK and occasionally overseas to attend meetings and conferences (if appropriate and with line manager approval)
Person Specification
Education/Qualifications
Desirable
* Knowledge of ICH/GCP guidelines
Education/Qualifications
Essential
* Educated to at least GCSE/A level (or equivalent)
Experience
Essential
* Experience in working with databases
Desirable
* Good understanding of medical terminology
* Previous experience of working in the NHS or equivalent
Skills/Abilities/Knowledge
Essential
* Excellent administrative and organisational skills
* Competence in research orientated PC software including Microsoft Office packages
* Excellent oral and written communication skills with the ability to work independently within a team environment
* Good attention to detail
* Good level of spoken and written English.
* Ability to grasp new concepts quickly and to have clear legible handwriting.
Desirable
* Understanding of clinical trials and regulations governing clinical research
* Experience of data entry and data management
Other Requirements
Essential
* Able to work on both sites and to be flexible to meet the needs of the role
Desirable
* Willingness to travel within UK and occasionally overseas to attend meetings and conferences (if appropriate and with line manager approval)
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Employer details
Employer name
The Royal Marsden NHS Foundation Trust
Address
The Royal Marsden Hospital
Sutton
SM2 5PT
Employer's website
(Opens in a new tab)
Employer details
Employer name
The Royal Marsden NHS Foundation Trust
Address
The Royal Marsden Hospital
Sutton
SM2 5PT
Employer's website
(Opens in a new tab)