Associate Regulatory Affairs Director

Astrazeneca

Base: $135,624.80 - $203,437.20 usd; bonus/equity:...
Regulatory submission strategy
Project management capabilities
Regulatory applications and procedures
The Associate Regulatory Affairs Director is responsible for leading the end-to-end planning, coordination, and execution of assigned deliverables, contributing to regulatory submission strategy and managing procedures through approval

Job Summary

  • The Associate Regulatory Affairs Director is responsible for leading the end-to-end planning, coordination, and execution of assigned deliverables, contributing to regulatory submission strategy and managing procedures through approval.
  • Responsibilities include understanding regulatory frameworks, providing expertise on procedural and documentation requirements, and leading cross-functional teams for major submissions.
  • AstraZeneca offers a competitive compensation package including base pay, bonus, equity, retirement contributions, and comprehensive benefits, with a minimum of three days per week in the office.

Matching Summary

The Associate Regulatory Affairs Director is responsible for leading the end-to-end planning, coordination, and execution of assigned deliverables, contributing to regulatory submission strategy and managing procedures through approval.

Salary

Base: $135,624.80 - $203,437.20 USD; Bonus/Equity: short-term incentive bonus, equity-based long-term incentive; Benefits: 401(k) plan, paid vacation and holidays, paid leaves, health benefits

Skills & Requirements

Must-have

  • regulatory submission strategy
  • project management capabilities
  • regulatory applications and procedures
  • regulatory expertise and guidance
  • drug development knowledge

Nice-to-have

  • bold thinking
  • inspire life-changing medicines
  • push boundaries in rare disease
  • transformative medicines
  • shaping the future of rare disease

Key Requirements

  • Bachelor's degree in science or related field
  • 4+ years regulatory experience
  • Extensive regulatory experience in biopharmaceutical industry
  • Thorough knowledge of drug development
  • Strong project management skills
  • Leadership skills

Work Rights

Not specified

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