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Senior Clinical Data Manager
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UK | Permanent | Sponsor-Dedicated CRO Position
We are looking for an experienced Clinical Data Management professional to join a sponsor-dedicated team supporting global clinical trials across gastrointestinal and neurology indications.
Working through a leading CRO, you will be fully embedded with the sponsor and act as the primary Data Management lead for complex studies. You’ll take ownership across the full clinical trial lifecycle, from study start-up through to database lock, while partnering with global cross-functional teams and external vendors.
Key Responsibilities
- Act as the primary Data Management lead on global clinical studies
- Lead activities from study start-up through to database lock
- Oversee EDC builds, system integrations and user acceptance testing
- Drive data review and reconciliation across EDC, laboratory, vendor, eCOA, IRT, and SAE data
- Manage external vendors and maintain strong stakeholder relationships
- Identify and resolve study risks, issues, and data-quality concerns
- Ensure compliance with CDISC standards, ICH-GCP, and regulatory requirements
- Support continuous improvement across Data Management processes
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Experience Required
- At least six years of experience in Clinical Data Management or Clinical Data Science
- Experience within a CRO or pharmaceutical environment
- Proven experience leading complex studies across the clinical trial lifecycle
- Strong data review and reconciliation experience
- Confident managing vendors and senior stakeholders
- Hands-on experience with EDC systems; Veeva EDC would be an advantage
- Knowledge of CDISC standards, including SDTM
- Strong understanding of clinical trial processes and ICH-GCP
- Excellent communication, problem-solving, and project leadership skills
- A relevant degree in Life Sciences, Health Sciences, or a related discipline
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Why Consider This Opportunity?
This position offers the chance to combine the variety and career opportunities of a CRO with the close partnership and ownership of a sponsor-embedded role. You’ll work on global studies in important therapeutic areas and have meaningful input from study set-up through to final database lock.
Applicants must have the legal right to work in the UK.
Interested? Apply now or get in touch
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