Transformative methods. Inquisitive minds. Life-changing foresight.
Clinical Data Manager
£38,000 – £43,000 plus benefits
Reports to: Data Management Operations Manager
Directorate: Research & Innovation
Contract: 24-month Fixed Term Contract
Hours: Full time, 35 hours per week or a 4 day week of 28 hours.
Location: Stratford, London (high flex 1‑2 days per week) or home based, UK (at request).
Closing date: Sunday 17th May 23:55pm
Interview date: Approximately first week of June 2026
Recruitment process: Competency based interview via Microsoft Teams + Data Management Task
Visa sponsorship: You must be eligible to work in the UK to apply for this vacancy. Cancer Research UK is not able to offer visa sponsorship.
Cancer Research UK (CRUK) is looking for a Clinical Data Manager to join the centre for Drug Development (CDD) on a 24‑month fixed term contract. CDD sponsors early phase and precision medicine clinical trials in oncology agents, with a portfolio rivaling that of a medium‑size pharmaceutical company. This is an exciting time as CDD expands its teams to maximize the impact of research for patients, with new international collaborations.
Responsibilities
* Lead the data management of assigned arms of the DETERMINE trial.
* Review the clinical trial data ensuring that data cleaning is managed effectively and efficiently, highlighting any issues that may affect data quality.
* Manage the development or amendment of clinical trial databases, reviewing eCRFs, specifying edit checks and performing validation.
* Facilitate the reporting of the data by managing the specification and validation of data listings and tables, coding adverse event terms and reconciling serious adverse events.
* Monitor the status of data entry and data cleaning, locking data when appropriate to protect data integrity.
* Work to achieve key performance indicators and project goals.
Qualifications
* Biomedical science graduate, nursing qualification holder or equivalent relevant experience.
* Proven knowledge and understanding of clinical data management and drug development, working to ICH/GCP and relevant legislation.
* Good knowledge and previous use of an electronic data capture (EDC) clinical trial database.
* Excellent written and verbal communication skills.
* Excellent attention to detail whilst retaining sight of the bigger picture.
* Good planning and organisational skills, able to prioritise and manage multiple competing tasks whilst working to challenging timelines.
* Experience of working on oncology trials is desirable.
Benefits: We provide a generous benefits package, career and personal development opportunities, and tools to support work‑life balance and personal wellbeing.
We actively encourage applications from people of all backgrounds and cultures, including ethnic minority backgrounds who are under‑represented. We cannot recruit anyone under the age of 18.
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