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

Trzdev37

Base: 128,488.00 to 168,640.50; bonus/equity: annu...
Fully remote
Quality management system (qms)
Ich-gcp compliance
Gxp-regulated environment
The Associate Director, Quality Management identifies, develops, tracks, and analyzes quality metrics and their impact on Late Development Oncology Clinical Operations

Job Summary

  • The Associate Director, Quality Management identifies, develops, tracks, and analyzes quality metrics and their impact on Late Development Oncology Clinical Operations.
  • The ADQM provides guidance on using business processes and existing systems to help Clinical Operations teams deliver drug and non-drug projects to agreed quality standards, maintaining an ‘always inspection-ready’ state.
  • Permanent positions offer an annual Variable Pay Bonus/Short Term Incentive opportunity as well as eligibility to participate in our equity-based long-term incentive program (if applicable to role).

Matching Summary

The Associate Director, Quality Management identifies, develops, tracks, and analyzes quality metrics and their impact on Late Development Oncology Clinical Operations.

Salary

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

Skills & Requirements

Must-have

  • Quality Management System (QMS)
  • ICH-GCP compliance
  • GxP-regulated environment
  • clinical trial delivery
  • international regulations and guidelines

Nice-to-have

  • strategic quality focus
  • engaging quality culture
  • proactive feedback seeking
  • good cultural awareness
  • global and remote teams

Key Requirements

  • Undergraduate degree in life sciences
  • In-depth knowledge pharmaceutical/biopharma industry
  • Excellent communication, influencing, networking skills
  • Strong critical thinking and sound judgment
  • Demonstrated stakeholder management skills
  • Strong risk-based decision-making skills
  • Excellent understanding drug development process
  • Strong understanding clinical study delivery
  • Excellent knowledge international regulations
  • Ability to collaborate proactively

Work Rights

Not specified

Tailored Resume

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