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

Trzdev28

Base: 128,488.00 to 168,640.50; bonus/equity: vari...
Fully remote
Quality management system (qms) framework
Ich-gcp compliance
Risk-based decision-making
The Associate Director, Quality Management provides guidance and support to ensure Late Development Oncology Clinical Operations maintain an 'always inspection-ready' state and deliver projects to agreed quality standards

Job Summary

  • The Associate Director, Quality Management provides guidance and support to ensure Late Development Oncology Clinical Operations maintain an 'always inspection-ready' state and deliver projects to agreed quality standards.
  • This role involves driving strategic quality focus, supporting compliance adherence, and leading quality review meetings to facilitate continuous improvement and sustainable issue resolution.
  • Permanent positions offer competitive benefits including a Flex Benefits & Retirement Savings Program, paid vacation, personal days, and eligibility for variable pay bonuses and equity-based long-term incentives.

Matching Summary

The Associate Director, Quality Management provides guidance and support to ensure Late Development Oncology Clinical Operations maintain an 'always inspection-ready' state and deliver projects to agreed quality standards.

Salary

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

Skills & Requirements

Must-have

  • Quality Management System (QMS) framework
  • ICH-GCP compliance
  • Risk-based decision-making
  • Clinical trial quality delivery
  • Stakeholder management skills
  • Cross-functional global collaboration

Nice-to-have

  • Experience with remote cross functional teams
  • Advanced degree in life sciences
  • Good cultural awareness
  • Ability to navigate ambiguity
  • Proactive knowledge sharing

Key Requirements

  • Undergraduate degree in life sciences
  • Experience in GxP-regulated pharmaceutical environment
  • Strong communication and influencing skills
  • Stakeholder management at all organizational levels
  • Excellent understanding of drug development and GxP activities
  • Knowledge of international regulations and AZ Procedural Framework

Work Rights

Not specified

Tailored Resume

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