Head, Clinical Trial Qa

Century Center

Not specified
Global clinical trial quality system
R&d quality management system
Gcp and cross functional consultancy
The Head of Clinical Trial Quality Assurance at CSL Behring is a leadership role responsible for overseeing the Global Clinical Trial Quality System, ensuring compliance and quality management across clinical development projects. The position entails strategic direction, management of quality assurance processes, and collaboration with cross-functional teams globally

Job Summary

  • The Head of Clinical Trial Quality Assurance role maintain and enhance the Global Clinical Trial Quality System supporting Early to Late-stage clinical development projects within R&D, utilizing and improving the existing R&D Quality Management System in alignment with CSL overarching Quality Management System administered and managed by Global Quality.
  • The role manages a Global Clinical quality department supporting early and late-stage clinical trials for all CSL business units across all R&D anchor sites.
  • CSL Behring is a global biotherapeutics leader driven by our promise to save lives.

Matching Summary

Match Score: 85

The Head of Clinical Trial Quality Assurance at CSL Behring is a leadership role responsible for overseeing the Global Clinical Trial Quality System, ensuring compliance and quality management across clinical development projects. The position entails strategic direction, management of quality assurance processes, and collaboration with cross-functional teams globally.

Skills & Requirements

Must-have

  • Global Clinical Trial Quality System
  • R&D Quality Management System
  • GCP and cross functional consultancy
  • Inspection management
  • GxP appropriate significant quality issues management

Nice-to-have

  • High ethical standards
  • Advocate for compliance and quality
  • Customer focus
  • Innovative business improvements

Key Requirements

  • Undergraduate degree (BA/BS) in Scientific discipline/Life Sciences or similar
  • 10+ years’ pharmaceutical company experience
  • Previous experience with inspection management preferred
  • Experience in Pharmacovigilance/GMP/Pre-Clinical related roles is desirable

Work Rights

Not specified

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