Associate Director Quality Management (late Development Oncology - Clinical Operations)

Trzdev36

Base: 128,488.00 to 168,640.50; bonus/equity: vari...
Fully remote
Quality management system (qms) framework
Ich-gcp compliance expertise
Risk-based decision-making skills
The Associate Director, Quality Management supports Late Development Oncology Clinical Operations by driving strategic quality focus and maintaining an ‘always inspection-ready’ state

Job Summary

  • The Associate Director, Quality Management supports Late Development Oncology Clinical Operations by driving strategic quality focus and maintaining an ‘always inspection-ready’ state.
  • This role offers a competitive salary range, annual variable pay bonus, equity-based long-term incentives, and comprehensive benefits including 4 weeks’ paid vacation and personal days.
  • The position emphasizes collaboration across global teams and continuous improvement of quality systems to ensure high-quality delivery of clinical trials.

Matching Summary

The Associate Director, Quality Management supports Late Development Oncology Clinical Operations by driving strategic quality focus and maintaining an ‘always inspection-ready’ state.

Salary

Base: 128,488.00 to 168,640.50; Bonus/Equity: Variable Pay Bonus and equity-based long-term incentive; Benefits: Flex Benefits, Retirement Savings, 4 weeks paid vacation, Personal Days

Skills & Requirements

Must-have

  • Quality Management System (QMS) framework
  • ICH-GCP compliance expertise
  • Risk-based decision-making skills
  • Clinical trial quality support
  • Cross-functional global collaboration
  • Regulatory inspection readiness

Nice-to-have

  • Experience with remote global teams
  • Strong cultural awareness
  • Advanced degree in life sciences
  • Proactive process improvement mindset
  • Stakeholder management skills

Key Requirements

  • Undergraduate degree in life sciences or related field
  • In-depth pharmaceutical/biopharma GxP experience
  • Excellent communication and influencing skills
  • Strong understanding of drug development and GxP activities
  • Knowledge of international regulations and AZ Procedural Framework

Work Rights

Not specified

Tailored Resume

Cover Letter