Senior Clinical Data Manager – Remote UK Leader

Warman O'Brien; Leeds; Remote; GBP 65,000 - 90,000; Full time

Job summary

Leading Global CRO in the UK is seeking a Senior Clinical Data Manager to own data management deliverables on remote, UK-wide projects. You will lead study builds, design eCRFs, manage timelines, and ensure data integrity across trials.

You'll mentor junior staff, coordinate with sponsors and auditors, and oversee QA processes during inspections. A strong background in CDM, regulatory knowledge (ICH-GCP), and hands-on data management is essential.

Qualifications

• Bachelor’s or Master’s degree in health/pharmaceutical sciences, physical/biological sciences, or chemistry fields (ICH-GCP familiarity is a plus).
• At least 5 years of pharmaceutical CDM experience or 2+ years as a CDM II with strong customer satisfaction track record.
• In-depth understanding of clinical trial data management, data standards, and regulatory guidance.

Responsibilities

• Own data management deliverables, timelines, and status reports for assigned projects.
• Serve as first line of contact for technical or scope discussions and participate in kickoff meetings and sponsor discussions.
• Plan study resources, mentor junior staff, and deliver training on EDC, dataflow, and QC processes.
• Maintain data management study binders and support audits and regulatory inspections.
• Lead study build/design, design eCRFs, participate in UAT, and ensure data integrity across trials.

Skills

Data management

Leadership

Regulatory knowledge

Project management

Education

Bachelor’s or Master’s degree in health/pharmaceutical sciences

Tools

EDC systems

Job description

Leading Global CRO in the UK is seeking a Senior Clinical Data Manager to own data management deliverables on remote, UK-wide projects. You will lead study builds, design eCRFs, manage timelines, and ensure data integrity across trials.

You'll mentor junior staff, coordinate with sponsors and auditors, and oversee QA processes during inspections. A strong background in CDM, regulatory knowledge (ICH-GCP), and hands-on data management is essential.