Senior Director, Cvrm Genomics Therapeutic Area Lead

Workatwamz

Not specified
Cvrm disease biology understanding
Apply human genetics to inform strategy
Lead cross-functional scientific teams
AstraZeneca is seeking a Senior Director for its Centre for Genomics Research to lead the Cardiovascular, Renal, and Metabolic (CVRM) Genomics Therapeutic Area. The role requires an MD and/or PhD in a relevant biomedical field, focusing on applying human genomics and multi-omic data to improve patient outcomes and guide therapeutic development

Job Summary

  • The Centre for Genomics Research is advancing one of the world’s most ambitious efforts to apply human genomics and population-scale health data to reshape how diseases are understood and how therapeutic decisions are made.
  • In this role, you will shape how human genetic and multi-omic evidence informs AstraZeneca’s strategy and pipeline in Cardiovascular, Renal, and Metabolic (CVRM) diseases.
  • AstraZeneca’s mission is to push the boundaries of science to deliver life-changing medicines.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Senior Director for its Centre for Genomics Research to lead the Cardiovascular, Renal, and Metabolic (CVRM) Genomics Therapeutic Area. The role requires an MD and/or PhD in a relevant biomedical field, focusing on applying human genomics and multi-omic data to improve patient outcomes and guide therapeutic development.

Skills & Requirements

Must-have

  • CVRM disease biology understanding
  • apply human genetics to inform strategy
  • lead cross-functional scientific teams
  • integrate multi-omic data
  • clinical trial design contribution

Nice-to-have

  • recognized scientific contributions
  • familiarity with regulatory considerations
  • mentoring and developing talent
  • collaborative and patient-centered leader

Key Requirements

  • MD and/or PhD in biomedical field
  • significant experience in clinical research/drug development
  • experience in genetic epidemiology/rare variant interpretation
  • proven track record leading complex teams
  • experience contributing to clinical trial design

Work Rights

Not specified

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