Head, Clinical Trial Qa

Chlworks

Not specified (assumed to be hybrid or flexible)
Global clinical trial quality system
R&d quality management system
Gcp and cross functional consultancy
The Head of Clinical Trial Quality Assurance at Chlworks is a strategic leadership role focused on enhancing the Global Clinical Trial Quality System to support R&D clinical development projects. The position requires significant experience in Quality Assurance and compliance within a pharmaceutical context, with a strong emphasis on managing quality processes across global clinical trials

Job Summary

  • The Head of Clinical Trial Quality Assurance role will maintain and enhance 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: 85

The Head of Clinical Trial Quality Assurance at Chlworks is a strategic leadership role focused on enhancing the Global Clinical Trial Quality System to support R&D clinical development projects. The position requires significant experience in Quality Assurance and compliance within a pharmaceutical context, with a strong emphasis on managing quality processes across global clinical trials.

Skills & Requirements

Must-have

  • Global Clinical Trial Quality System
  • R&D Quality Management System
  • GCP and cross functional consultancy
  • Inspection management
  • Significant Issue / Serious Breach Management
  • Deviation and CAPA Management

Nice-to-have

  • Strategic leadership
  • Continuous improvement initiatives
  • Global cross functional teams
  • Mentoring and coaching staff

Key Requirements

  • Undergraduate degree in Scientific discipline/Life Sciences
  • 10+ years pharmaceutical company experience
  • Experience with inspection management
  • Experience in Pharmacovigilance/GMP/Pre-Clinical roles desirable
  • Experience in pre-clinical/clinical regulations

Work Rights

Not specified

Tailored Resume

Cover Letter