Senior Clinical Data Manager

AL Solutions; United Kingdom; Remote; GBP 70,000 - 100,000; Full time

Job summary

AL Solutions is seeking a Senior Clinical Data Manager in the United Kingdom to lead end-to-end data management on an FSP project for an international pharmaceutical sponsor within the Neurology & GI unit. The role is remote from the UK with flexible start dates.

You will act as the primary data lead in cross-functional study teams, oversee start-up activities (EDC build, UAT, system integrations), data review, data reconciliation, vendor oversight and database lock readiness, while ensuring

Qualifications

• 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).

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.

Skills

Data management

Clinical trials

CDISC

Veeva

Regulatory knowledge

Education

Bachelor's in life sciences

Tools

Veeva

Job description

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)