Associate Director, Process & Documentation

AstraZeneca

Base: $143,112.80 - $214,669.20; bonus/equity: sho...
**
Clinical data management process development
Six sigma methodology application
Gxp and ha compliance oversight
** AstraZeneca is seeking an Associate Director for Process & Documentation in Data Management, responsible for enhancing business operations and driving process improvements. The role requires expertise in clinical data management, project management, and effective communication with stakeholders. **

Job Summary

  • The role is responsible for promoting and branding Data Management while ensuring the efficiency of business operations through process simplification.
  • Candidates must possess a Six Sigma Green Belt certification to apply best practices and drive continuous process improvements within the function.
  • The position offers a competitive base pay ranging from $143,112.80 to $214,669.20 along with comprehensive benefits including health coverage and retirement plans.

Matching Summary

Match Score: 75

** AstraZeneca is seeking an Associate Director for Process & Documentation in Data Management, responsible for enhancing business operations and driving process improvements. The role requires expertise in clinical data management, project management, and effective communication with stakeholders. **

Salary

Base: $143,112.80 - $214,669.20; Bonus/Equity: Short-term incentive bonus and equity-based long-term incentive program available; Benefits: 401(k), paid vacation, holidays, leaves, medical, dental, vision

Skills & Requirements

Must-have

  • Clinical Data Management process development
  • Six Sigma methodology application
  • GxP and HA compliance oversight
  • SOP stewardship and training
  • Cross-functional stakeholder collaboration

Nice-to-have

  • Social media content creation skills
  • Video production capabilities
  • Strategic business analytics ability
  • Mentoring and coaching experience
  • Innovative outside-the-box thinking

Key Requirements

  • Bachelor's degree in scientific discipline or related field
  • 5+ years of experience in pharmaceutical, biotech, CRO, or Regulatory Agency
  • Six Sigma Green Belt certification required
  • Strong understanding of GCP, ICH, and GCDMP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter