Senior Clinical Data Manager

We are currently searching for a Senior Clinical Data Manager in the UK to work on an FSP project to an international Pharma, within their Neurology & GI business unit.

This position will be focused on leading studies across cross-functional study teams within the sponsor, covering end-to-end data management tasks.

The location is limited to remote workers in the UK with flexible start dates being offered.

Responsibilities:

• Act as the primary data lead within cross-functional study teams
• Lead study start-up activities by coordinating EDC build & configuration, system integrations, user acceptance testing (UAT), and the timely completion of key data management milestones.
• Manage ongoing data review processes, reconciliation activities, vendor oversight, and database lock readiness to maintain data quality and study timelines.
• Maintained adherence to CDISC standards, ICH-GCP guidelines, and applicable regulatory requirements throughout the clinical trial lifecycle.
• Proactively assess and address project risks while implementing process improvements to enhance operational efficiency and overall data management quality.

Experience

Required:

• Proven track record working in data management within clinical trials
• Previous experience independently leading studies
• Knowledge of CDISC standards
• Strong understanding of the clinical trial process, regulatory requirements, and ICH-GCP
• Strong hands-on experience with EDC systems (Veeva preferred)