Remote Clinical Data Manager — Lead & Train UK

Warman O'Brien

United Kingdom

Remote

GBP 70,000 - 95,000

Full time

32 hours ago
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Job summary

Warman O'Brien is seeking a Clinical Data Manager for a fully remote role based in the UK. You will own data management deliverables, lead eCRF design and data cleaning, and mentor junior staff while coordinating with clients and QA during audits.

This position emphasizes strong leadership within a flexible, home-based environment, with responsibility for study-level planning and regulatory compliance across global projects.

Qualifications

  • Bachelor's or Master's degree in health/pharmaceutical or related sciences.
  • 3–5 years of pharmaceutical CDM experience.
  • Deep understanding of ICH-GCP and data standards.
  • Proven leadership in CDM activities.

Responsibilities

  • Act as primary owner of data management deliverables, timelines, and status reports.
  • Serve as first point of contact for technical or scope discussions during projects.
  • Plan study resources and mentor junior staff; deliver training on EDC systems and data QC.
  • Support audits and regulatory inspections with Study Binders and QA documentation.
  • Lead study build and design, annotated CRFs, and UAT participation.
  • Develop and maintain DMP, Data Management Project Plan, and DQRP.
  • Oversee data review, query resolution, and SAE reconciliation, including vendor data streams.
  • Manage post-go-live database changes, locks, and archival coordination.

Skills

Leadership
Data management
EDC systems
Regulatory compliance

Education

Bachelor's or Master's in life sciences

Tools

EDC platforms
UAT testing tools

Job description

Warman O'Brien is seeking a Clinical Data Manager for a fully remote role based in the UK. You will own data management deliverables, lead eCRF design and data cleaning, and mentor junior staff while coordinating with clients and QA during audits.

This position emphasizes strong leadership within a flexible, home-based environment, with responsibility for study-level planning and regulatory compliance across global projects.

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