Clinical Regulatory Writer (associate Director Or Manager)

AstraZeneca

Boston, MA, US
Base: $133,042.40 - $199,563.60 usd (assoc dir); $...
3d onsite
7+ years medical writing experience
Bs life sciences degree required
Hybrid work model 3 days onsite
This role involves independently managing complex clinical regulatory writing activities and authoring strategic documents for drug development

Job Summary

  • This role involves independently managing complex clinical regulatory writing activities and authoring strategic documents for drug development.
  • The position offers the opportunity to drive continuous improvement and operational excellence while collaborating with global functions.
  • Employees are eligible for short-term incentive bonuses, equity-based awards, and comprehensive health and retirement benefits.

Matching Summary

This role involves independently managing complex clinical regulatory writing activities and authoring strategic documents for drug development.

Salary

Base: $133,042.40 - $199,563.60 USD (Assoc Dir); $113,293.60 - $169,940.40 USD (Mgr); Bonus/Equity: Short-term incentives and equity available; Benefits: Retirement programs, PTO, health/dental/vision

Skills & Requirements

Must-have

  • 7+ years medical writing experience
  • BS Life Sciences degree required
  • Hybrid work model 3 days onsite

Nice-to-have

  • Advanced scientific degree (Ph.D.)
  • Experience leading clinical submissions
  • Strategic thinking and review capabilities

Key Requirements

  • Associate Director: 7+ years experience
  • Manager level: 2-7+ years experience
  • In-depth knowledge of CTD module requirements

Work Rights

Not specified

Tailored Resume

Cover Letter