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Senior Research Data Manager
| Posting date: | 05 January 2026 |
|---|---|
| Salary: | £37,259.00 to £45,356.00 per year |
| Additional salary information: | £37259.00 - £45356.00 a year |
| Hours: | Full time |
| Closing date: | 18 January 2026 |
| Location: | London, SE59RS |
| Company: | NHS Jobs |
| Job type: | Contract |
| Job reference: | C9213-26-0004 |
Summary
1Data Management Ensure accurate and timely completion of Case Report Forms (CRFs) according to trial protocol Responsible for the collection, co-ordination and computerisation of data generated from the clinical trials. Maintain the Trial Master file (TMF) and Investigator Site File (ISF) with essential documents and version control. Prompt query resolution Ensure SAEs are recorded and reported in accordance with the protocol and/or sponsors SOP. Liaise with other departments and wards at the site/s, to promote a good working environment, integration of research within and open channels of communication. Inform appropriate medical personnel and departments of portfolio of clinical trials. Report adverse incidents and near misses via the Trusts online incident reporting form. To contribute to the development, review and maintenance of Standard Operating Procedures (SOP). Support internal and external monitoring and audit activities related to clinical research Uphold the principles of Good Clinical Practice (GCP) and all relevant clinical trial regulations. Act as a resource and support to patients and their relatives when required Obtain Informed consent for registry studies and provide cross site cover as required. 2Governance / Quality Control Work in accordance with all regulatory requirements including: Local Standard Operating Procedures Good Clinical Practice Medicines for Human Use (Clinical Trials) Regulations Research Governance Framework for Health and Social Care Human Tissue Act Administrative Responsibilities Provide comprehensive administrative support for research meetings, including agenda preparation, minute taking, and follow-up actions. Complete case report forms in a precise and timely manner, ensuring that all the relevant clinical data in the patients medical notes and trial file is transcribed accurately. To update the Trial Manager /Clinical Trials Coordinator regularly the status of such data Assist in preparing and submitting documentation to ethics committees, regulatory authorities and R&D. Create and maintain the file of current protocols and patient information sheets, ensuring version control. Be responsible for the maintenance of the Investigator Site Files. Develop, update, and maintain trial-specific databases and electronic worksheets. Formulate and maintain the databases for clinical trials. Organise and prepare documentation for audit and monitoring visits. Provide cover when necessary for colleagues during periods of absence. Clinical Responsibilities Conduct patient facing activities to include obtaining informed consent for registry studies. Perform sample processing and shipping Carry our basic clinical tasks such as phlebotomy and vital signs