Job Summary

• The Associate Director, Quality Management provides guidance and support to ensure high-quality delivery of clinical trials within Late Development Oncology Clinical Operations.
• This role champions an engaging quality culture promoting an ‘always inspection-ready’ mindset and drives continuous improvement through collaboration with stakeholders and quality partners.
• The position offers a competitive salary range with bonus and equity opportunities, flexible benefits, retirement savings, paid vacation, and personal days.

Matching Summary

Salary

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

Skills & Requirements

Key Requirements

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

Work Rights