Executive Medical Director, Hematology

AstraZeneca

Boston, MA, USA
Base: 323,216.00 - 484,824.00 usd annual; bonus/eq...
Hematology clinical development leadership
Oversee 2 or more programs
Medical expert for study teams
The Executive Medical Director role is responsible for overseeing 2 or more programs, providing oversight/guidance/mentoring to Medical Directors and Clinical Development Scientists, and serving on cross-asset strategic teams

Job Summary

  • The Executive Medical Director role is responsible for overseeing 2 or more programs, providing oversight/guidance/mentoring to Medical Directors and Clinical Development Scientists, and serving on cross-asset strategic teams.
  • This specialized role provides medical leadership and input to Program Teams during early to late stage drug development, serving as a medical expert and potentially as a medical monitor for clinical trials.
  • The position offers substantial opportunities for scientific and commercial interactions and career advancement in the fast-moving area of rare disease.

Matching Summary

The Executive Medical Director role is responsible for overseeing 2 or more programs, providing oversight/guidance/mentoring to Medical Directors and Clinical Development Scientists, and serving on cross-asset strategic teams.

Salary

Base: 323,216.00 - 484,824.00 USD Annual; Bonus/Equity: Short-term incentive bonus opportunity, equity-based long-term incentive program; Benefits: Qualified retirement program [401(k) plan], paid vacation and holidays, paid leaves, health benefits

Skills & Requirements

Must-have

  • Hematology clinical development leadership
  • Oversee 2 or more programs
  • Medical expert for study teams
  • Lead cross-functional teams
  • Manage benefit to risk profile
  • Scientific and medical input

Nice-to-have

  • Scientific and commercial interactions
  • Career advancement opportunities
  • Rare disease expertise
  • Foster development of Medical Directors

Key Requirements

  • MD or equivalent
  • 7+ years clinical development experience
  • Global regulatory expertise
  • Product development expertise
  • Experience with FDA meetings
  • Experience designing multinational trials
  • Experience supporting business development

Work Rights

Not specified

Tailored Resume

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