Clinical Scientist Director, Late Development- Inflammation

Amgen Australia Pty Ltd

Base: 229,458.00 usd - 273,757.00 usd; bonus/equit...
Not specified
Late-phase clinical development
Protocol execution
Medical data review
Amgen Australia Pty Ltd is seeking a Clinical Scientist Director for Late Development in Inflammation. The role involves overseeing late-phase clinical development, ensuring protocol execution and data integrity while collaborating with cross-functional teams

Job Summary

  • The Clinical Scientist Director will support late-phase clinical development by translating scientific and clinical strategy into actionable execution across clinical trials.
  • The Clinical Scientist serves as a key clinical development team member, providing hands-on oversight of protocol execution, medical data review, and clinical data quality to enable high-quality, decision-ready data.
  • Amgen offers a comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

Matching Summary

Match Score: 85

Amgen Australia Pty Ltd is seeking a Clinical Scientist Director for Late Development in Inflammation. The role involves overseeing late-phase clinical development, ensuring protocol execution and data integrity while collaborating with cross-functional teams.

Salary

Base: 229,458.00 USD - 273,757.00 USD; Bonus/Equity: Discretionary annual bonus program, Stock-based long-term incentives; Benefits: Comprehensive employee benefits package

Skills & Requirements

Must-have

  • late-phase clinical development
  • protocol execution
  • medical data review
  • clinical data quality
  • cross-functional teams
  • Inflammation Development Therapeutic Area

Nice-to-have

  • scientific and clinical strategy
  • collaborative culture
  • science based
  • passion for challenges

Key Requirements

  • Doctorate degree and 4 years of clinical development experience
  • Master’s degree and 7 years of clinical development experience
  • Bachelor’s degree and 9 years of clinical development experience
  • 5 years of pharmaceutical clinical drug development experience
  • Proven track record of clinical trial process improvement
  • Industry or academic experience in late-phase drug development
  • Strong communication & presentation skills
  • Experience with designing, monitoring, and implementing clinical trials
  • Understanding of conducting study data readout activities
  • Experience drafting high level submission documents
  • Serving as a contributing author to scientific publications
  • Experience in clinical data analysis

Work Rights

Not specified

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