Global Development Senior Medical Director, Hematology Oncology

AstraZeneca

Gaithersburg, Maryland, United States
Base: $288,059.20 - $432,088.80; bonus/equity: sho...
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Md or international equivalent required
Medical hemato-oncology clinical training
4 years relevant drug development experience
** AstraZeneca is seeking a Senior Medical Director for Global Development in Hematology Oncology, responsible for leading clinical trial strategies and ensuring patient safety. The role requires strong collaboration and communication skills, with a focus on drug development and regulatory compliance. **

Job Summary

  • This role is critical for advancing the science to deliver life-changing medicines to patients with hematological cancers through a combination-focused pipeline.
  • The Senior Global Development Medical Director will lead the design, implementation, and safety monitoring of early and late-phase clinical trials while ensuring compliance with FDA, EMEA, ICH, and GCP guidelines.
  • AstraZeneca offers a competitive compensation package including an annual base pay range of $288,059.20 - $432,088.80, short-term incentives, equity-based long-term incentives, and comprehensive health benefits.

Matching Summary

Match Score: 75

** AstraZeneca is seeking a Senior Medical Director for Global Development in Hematology Oncology, responsible for leading clinical trial strategies and ensuring patient safety. The role requires strong collaboration and communication skills, with a focus on drug development and regulatory compliance. **

Salary

Base: $288,059.20 - $432,088.80; Bonus/Equity: Short-term incentive bonus and equity-based long-term incentive program available; Benefits: Qualified retirement program, paid vacation, holidays, leaves, and health coverage

Skills & Requirements

Must-have

  • MD or international equivalent required
  • Medical hemato-oncology clinical training
  • 4 years relevant drug development experience
  • Board Certification preferred
  • Good Clinical Practice (GCP) knowledge
  • Clinical trial design and implementation
  • Regulatory submission expertise

Nice-to-have

  • Strong collaborative communication skills
  • Mentoring less experienced staff
  • Experience with in-licensing due diligence
  • Cross-functional leadership abilities
  • Innovative process improvement mindset

Key Requirements

  • MD or international equivalent
  • Medical hemato-oncology clinical training
  • Minimum 4 years relevant experience
  • Board Certification preferred
  • Detailed knowledge of GCP regulations

Work Rights

Not specified

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