Senior Director, Cvrm Genomics Therapeutic Area Lead

Zse68

Not specified
Cvrm disease biology understanding
Apply human genetics to inform strategy
Lead cross-functional scientific teams
AstraZeneca is seeking a Senior Director for the Cvrm Genomics Therapeutic Area Lead position within its Centre for Genomics Research. The ideal candidate will hold an MD and/or PhD, possess extensive experience in CVRM disease biology, and have a proven track record in clinical research or drug development

Job Summary

  • The Centre for Genomics Research (CGR) 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.
  • An inclusive culture that champions diversity and collaboration, we are committed to lifelong learning, growth and development.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Senior Director for the Cvrm Genomics Therapeutic Area Lead position within its Centre for Genomics Research. The ideal candidate will hold an MD and/or PhD, possess extensive experience in CVRM disease biology, and have a proven track record in clinical research or drug development.

Skills & Requirements

Must-have

  • CVRM disease biology understanding
  • apply human genetics to inform strategy
  • lead cross-functional scientific teams
  • integrate multi-omic evidence
  • patient selection and stratification

Nice-to-have

  • recognized scientific contributions
  • familiarity with regulatory considerations
  • lifelong learning and growth
  • entrepreneurial spirit

Key Requirements

  • MD and/or PhD in relevant 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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