£33,100 Per year
Undetermined
Undetermined
Sutton, England, United Kingdom
Summary: The Clinical Data Manager role involves the collection and transcription of clinical trial data, communication with study teams and sponsors, and maintaining study-specific files. Candidates should have a health or science-related qualification or relevant experience in clinical trials, along with strong organizational and communication skills. The position is based at the Drug Development Unit at The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, focusing on early-phase oncology trials. This is a full-time, 12-month contract position with a salary range of £31,445 to £33,100 per annum.
Key Responsibilities:
- Collation and collection of clinical data.
- Transcription of clinical trial data into trial-specific databases.
- Communication with the study team and study sponsors.
- Developing tools to support protocol-specific data capturing.
- Maintaining study-specific files and archiving studies.
- Working with the team for study audits.
- Supporting the study team in meeting data locks.
Key Skills:
- Health/science-related higher education qualification or relevant experience in clinical trials.
- Excellent organizational skills.
- Strong interpersonal and communication skills.
- High level of time management skills.
- Computer literate.
- Previous experience in oncology or clinical trial research preferred.
- Extensive experience in healthcare administration.
Salary (Rate): £33,100 yearly
City: Sutton
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Salary: £31,445- £33,100 per annum. Commencement on the salary range is subject to comparable skills and experience. Duration of Contract : 12 months in the first instance Hours per week : 35 hours per week (Full Time) Closing Date : 23rd of April 2026, this may close early if there is a high volume of applicants. The post involves collation and/or collection of clinical data, transcription of clinical trial data into trial specific databases, communication with the study team and study sponsors, developing tools to support protocol specific data-capturing, maintaining study specific files, archive the studies, work with team for study audits, and support study team in meeting data locks. The role requires familiarity with medical terminology and a comprehensive approach to processing trial data and also ability to work under pressure. Key Requirements Applications are invited from candidates with a health/science related higher education qualification or relevant experience in clinical trials, who possess excellent organisational skills, strong interpersonal and communication skills and high level of time management skills. The successful candidate will be computer literate and will preferably have previous experience in oncology or clinical trial research or extensive experience in healthcare administration. Appointments will be on a one-year contract in the first instance. To apply for this post, please submit an online application including a supporting statement, detailing reasons why you are applying for the post and with your CV. We encourage all applicants to access the job pack attached for more detailed information regarding this role. Due to the high volumes of applications we receive, we reserve the right to close the advert before the published closing date once we have received a sufficient number of applications. Therefore, we advise that you to submit your application, as early as possible to avoid disappointment. Department/Directorate Information The Drug Development Unit, (DDU) at The Institute of Cancer Research, London, and The Royal Marsden NHS Foundation Trust, is a world-leading centre for early-phase oncology trials, translating cutting-edge science into first-in-human clinical trials. Through close integration of laboratory and clinical expertise, the Unit supports the functions of sponsoring early phase trials through Investigator Initiated Trials Team, as well as, delivers academic and industry sponsored trials. Our mission is to fast-track the development of anti-cancer drugs, designed and synthesised at the Institute of Cancer Research, or developed by CRUK scientists, or developed by industry collaborators, in order to rapidly impact the care of cancer patients. The DDU has been involved in the development of many hundreds of novel agents including several practice-changing cancer drugs. The DDU is one of the Experimental Cancer Medicine Centres in the UK, part of the CRUK Convergence Science Centre and the Early Phase Drug Development Theme within the ICR-RM NIHR Biomedical Research Centre (BRC). The DDU has multiple academic and industry collaborations both nationally and internationally, to optimally serve our patients. The Unit is led by Professor Johann de Bono and Professor Udai Banerji. Why work for us? As a member of staff, you'll have exclusive access to a range of staff benefits. The ICR is committed to supporting overseas applicants applying for roles, please click here to find out further information. The Institute of Cancer Research, London, is one of the world's most influential cancer research institutes, with an outstanding record of achievement dating back more than 100 years. Further information about working at the ICR can be found here . We look forward to receiving applications from all candidates, wherever in the world they are currently based. We will select those who display the potential to become, or to support, the world leading cancer researchers of the future based on their application and performance at interview. However, we particularly welcome British applicants from black and ethnic minority backgrounds, as they are under-represented within the ICR and nationwide in STEM roles.