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
Hematology oncology clinical training required
4+ years relevant drug development experience
** AstraZeneca is seeking a Senior Medical Director for Global Development in Hematology Oncology, ideally based in Gaithersburg, Boston, South San Francisco, or Barcelona. The role requires a medical degree and extensive experience in clinical research, with a focus on drug development in oncology and hematology. **

Job Summary

  • This role is critical for advancing the science to deliver life-changing medicines for patients with hematological cancers through a combination-focused pipeline.
  • The Senior Global Development Medical Director will lead clinical project teams in designing, executing, and closing complex hemato-oncology studies while ensuring patient safety and regulatory compliance.
  • AstraZeneca offers a competitive compensation package including base pay ranging from $288,059.20 to $432,088.80, short-term incentives, equity-based long-term programs, and comprehensive health benefits.

Matching Summary

Match Score: 75

** AstraZeneca is seeking a Senior Medical Director for Global Development in Hematology Oncology, ideally based in Gaithersburg, Boston, South San Francisco, or Barcelona. The role requires a medical degree and extensive experience in clinical research, with a focus on drug development in oncology and hematology. **

Salary

Base: $288,059.20 - $432,088.80; Bonus/Equity: Short-term incentive bonus and equity-based long-term incentive program available; Benefits: 401(k), paid vacation, holidays, leaves, medical, dental, vision coverage

Skills & Requirements

Must-have

  • MD or international equivalent required
  • Hematology oncology clinical training required
  • 4+ years relevant drug development experience
  • Board certification preferred
  • Expertise in GCP and regulatory compliance
  • Clinical trial design and implementation
  • Safety monitoring for Phase I-III studies

Nice-to-have

  • Strong cross-functional collaboration skills
  • Mentoring less experienced staff
  • Experience with in-licensing due diligence
  • Ability to influence diverse stakeholders
  • Knowledge of reimbursement requirements

Key Requirements

  • MD or international equivalent degree
  • Medical hemato-oncology clinical training
  • Minimum 4 years industry experience
  • Board certification (preferred)
  • Detailed knowledge of FDA/EMEA regulations

Work Rights

Not specified

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