Head, Clinical Trial Qa

csl.co.th

**
Global clinical trial quality system
R&d quality management system
Gcp and cross functional consultancy expertise
** CSL Behring is seeking a Head of Clinical Trial Quality Assurance to oversee and improve the Global Clinical Trial Quality System in support of clinical development projects. The ideal candidate will have extensive experience in quality assurance and compliance within the pharmaceutical industry, particularly in clinical trials. **

Job Summary

  • The Head of Clinical Trial Quality Assurance role maintains and enhances the Global Clinical Trial Quality System supporting Early to Late-stage clinical development projects within R&D.
  • This position strategically oversees aspects of the R&D Quality Management in relation to key quality elements such as Document Management, Knowledge Management, Significant Issue / Serious Breach Management, Deviation and CAPA Management, Risk Management, Continuous Improvement, Inspection Management, Change Management and R&D Quality Governance associated with R&D clinical development.
  • CSL Behring is a global biotherapeutics leader driven by our promise to save lives, focused on serving patients’ needs by using the latest technologies.

Matching Summary

Match Score: 75

** CSL Behring is seeking a Head of Clinical Trial Quality Assurance to oversee and improve the Global Clinical Trial Quality System in support of clinical development projects. The ideal candidate will have extensive experience in quality assurance and compliance within the pharmaceutical industry, particularly in clinical trials. **

Skills & Requirements

Must-have

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

Nice-to-have

  • High ethical standards and credibility
  • Visible and credible advocate for compliance
  • Customer focus and strong organization

Key Requirements

  • Undergraduate degree in Scientific discipline/Life Sciences
  • 10+ years pharmaceutical company experience
  • Previous experience with inspection management
  • Experience in pre-clinical/clinical regulations

Work Rights

Not specified

Tailored Resume

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