Global Clinical Data Lead (Sponsor-Embedded Trials)

Meet Life Sciences Ltd.; United Kingdom; On-site; GBP 65,000 - 85,000; Full time

Job summary

Meet Life Sciences Ltd. in the United Kingdom is seeking an experienced Clinical Data Management professional to join a sponsor-dedicated team supporting global trials across GI and neurology indications.

You’ll be the primary Data Management lead for complex studies, owning the lifecycle from startup to database lock and collaborating with global cross-functional teams and external vendors. This role requires at least six years in CDM or data science, CRO/pharma experience, and proven

Qualifications

• Six+ years in Clinical Data Management or Clinical Data Science.
• Experience in CRO or pharmaceutical environments.
• Proven leadership of complex studies across the lifecycle.
• Strong data review and reconciliation experience.
• Experience managing vendors and senior stakeholders.
• Hands-on EDC experience; Veeva EDC advantageous.
• Knowledge of CDISC standards, including SDTM.
• Understanding of clinical trial processes and ICH-GCP.
• Excellent communication, problem-solving and leadership skills.
• Relevant life sciences degree or related discipline.

Responsibilities

• Act as the primary Data Management lead on global clinical studies
• Lead activities from study start-up through to database lock
• Oversee EDC builds, system integrations and user acceptance testing
• Drive data review and reconciliation across EDC, laboratory, vendor, eCOA, IRT and SAE data
• Manage external vendors and maintain stakeholder relationships
• Identify and resolve study risks, issues and data-quality concerns
• Ensure compliance with CDISC standards, ICH-GCP and regulatory requirements

Skills

Clinical Data Mgmt

Data reconciliation

Veeva EDC

CDISC SDTM

ICH-GCP

Vendor management

Lifecycle leadership

Regulatory compliance

Stakeholder management

Communication skills

Education

Bachelor's degree in Life Sciences

Tools

Veeva EDC

Job description

Meet Life Sciences Ltd. in the United Kingdom is seeking an experienced Clinical Data Management professional to join a sponsor-dedicated team supporting global trials across GI and neurology indications.

You’ll be the primary Data Management lead for complex studies, owning the lifecycle from startup to database lock and collaborating with global cross-functional teams and external vendors. This role requires at least six years in CDM or data science, CRO/pharma experience, and proven