Senior Clinical Data Manager - Remote Lead

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

Job summary

Leading Global CRO is seeking a Senior Clinical Data Manager for a fully remote UK role. You will lead data management activities, own project data deliverables, manage client relationships, and mentor junior staff across studies.

The role requires 5+ years in pharmaceutical data management (or 2+ years as CDM II), strong knowledge of ICH-GCP, data standards, and QA processes. Flexible, home-based work with global trial oversight.

Qualifications

• Education in health/pharmaceutical sciences, physical/biological sciences or chemistry.
• 5+ years in pharma clinical trial data management or 2+ years as CDM II.
• Strong knowledge of ICH-GCP and data standards.
• Demonstrated leadership in CDM activities and project delivery.

Responsibilities

• Own data management deliverables, timelines, and reports for assigned projects.
• Serve as first line of contact for technical/ scope discussions and client meetings.
• Plan study resources and mentor junior staff; deliver training on EDC, dataflow, QC.
• Maintain study binders and support during client audits and regulatory inspections.
• Lead eCRF design, annotated CRFs, and participate in database design/UAT.
• Develop and maintain essential study documents (DMP, project plan, DQRP).
• Oversee data cleaning, SAE reconciliation, and data-stream integration.
• Coordinate post-go-live modifications and archival documentation.

Skills

Leadership

Project management

Data management

Training

Regulatory knowledge

Communication

Education

Bachelor's or Master's in health/pharmaceutical sciences/chemistry

Tools

EDC systems

User Acceptance Testing (UAT)

Job description

Leading Global CRO is seeking a Senior Clinical Data Manager for a fully remote UK role. You will lead data management activities, own project data deliverables, manage client relationships, and mentor junior staff across studies.

The role requires 5+ years in pharmaceutical data management (or 2+ years as CDM II), strong knowledge of ICH-GCP, data standards, and QA processes. Flexible, home-based work with global trial oversight.