Location
London, United Kingdom
Type
Full Time
Salary (£)
54,320 to 60,981 per year
About Barts Health NHS Trust
Barts Health NHS Trust is part of one of the largest NHS Trusts in the UK. Their work fuels the future of healthcare through leading-edge research and deep partnerships with academic institutions like Queen Mary University of London. As part of their Joint Research Management Office, they support high-impact clinical trials that improve lives across the globe. If you’re passionate about data integrity, clinical research, and building better systems for tomorrow, you’ll find real purpose here.
Job details
Benefits
- Visa sponsorship for skilled workers, making relocation smoother
- Supportive work environment with cross-team collaboration across NHS and academic research bodies
- Training opportunities in Good Clinical Practice (GCP) and REDCap systems
- Career growth through leadership of newly established functions
- Flexible working arrangements in a research-focused setting
Requirements
- A degree or equivalent in a relevant subject
- Solid experience overseeing clinical trials databases, especially in MHRA-regulated research
- Proficiency in programming and database development
- Hands-on knowledge of GCP, GDPR, and the Data Protection Act 2018
- Comfortable using REDCap and writing SQL queries
- Ability to explain complex data outcomes to non-technical stakeholders
- Skilled in drafting and reviewing Data Management Plans and system specifications
Salary Details
They’re offering between £54,320 and £60,981 per year, depending on experience and qualifications.
About the Role
This is more than just a technical role. You’ll be the go-to person for building and validating research databases used in clinical trials, particularly those regulated by the MHRA. You’ll work closely with the Research IT Services and Data Warehouse Team, guiding database compliance from concept through delivery. A big part of the role involves training others, reviewing system use, and leading Sponsor oversight. There’s a clear opportunity here to shape how clinical data is handled across two major UK institutions.
It’s ideal for someone who’s already built compliant databases and now wants to step into a leadership space, influence data practices, and make a difference to how health research is delivered.
Key Responsibilities
- Lead design, testing, and validation of clinical research databases that meet MHRA compliance
- Drive optimisation of tools like REDCap, ensuring efficient and ethical data capture
- Oversee multiple live projects, hitting key milestones with strong documentation
- Provide Sponsor oversight for clinical trials and ensure compliance with GCP
- Write and review complex Requirement Specification Documents and SOPs
- Select and assess vendors offering MHRA-compliant systems
- Collaborate across university and NHS teams to keep standards high
Disclosure and Barring Service Check
This role requires a standard Disclosure and Barring Service (DBS) check due to its involvement with sensitive research data and systems.
Certificate of Sponsorship
Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website.
Equal Opportunity Statement
They’re committed to being an inclusive employer. All qualified applicants will be considered fairly, regardless of background, gender, age, or disability.
Employer Details
- Company Name: Barts Health NHS Trust
- Address: London, United Kingdom
- Contact: Available upon request or via NHS Jobs
Reference Number
This job is listed under the internal reference system for tracking and application management.
How To Apply
Ready to step into a role that combines purpose, data, and impact? Apply now to start your journey with a team that values your expertise and supports your growth.
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