Statistical Programming Associate Director (cvrm)

AstraZeneca

Warsaw, Poland
Hybrid (3 days in office, 2 remote)
Statistical programming leadership
Clinical drug development knowledge
Sas programming skills
AstraZeneca is seeking a Statistical Programming Associate Director to join their Cardiovascular Renal Metabolism (CVRM) Biometrics team in Warsaw, Poland. The role focuses on leading programming efforts in clinical drug development, requiring extensive programming experience and knowledge of industry standards. The position offers hybrid work flexibility, professional growth opportunities, and a collaborative work environment

Job Summary

  • This role is a delivery focused technical leadership role for programming and overseeing deliverables with quality and timeliness, following established standards and processes.
  • You will provide subject matter expertise within the Programming discipline and act as a specialist within cross-functional teams to deliver continuous improvement.
  • At AstraZeneca, we believe in the potential of our people, and you will develop beyond what you thought possible.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Statistical Programming Associate Director to join their Cardiovascular Renal Metabolism (CVRM) Biometrics team in Warsaw, Poland. The role focuses on leading programming efforts in clinical drug development, requiring extensive programming experience and knowledge of industry standards. The position offers hybrid work flexibility, professional growth opportunities, and a collaborative work environment.

Skills & Requirements

Must-have

  • Statistical programming leadership
  • Clinical drug development knowledge
  • SAS programming skills
  • CDISC industry standards
  • Cross-functional team collaboration

Nice-to-have

  • Agile global team environment
  • Strategic impact on drug development
  • Continuous improvement initiatives
  • Mentorship and training

Key Requirements

  • Degree in Mathematics, Statistics, Computer Science, Life Science, or equivalent
  • Excellent SAS (or R) and SAS macros programming skills
  • Thorough knowledge of the clinical development process
  • Thorough knowledge of industry standards (CDISC)
  • Current knowledge of technical and regulatory requirements

Work Rights

Not specified

Tailored Resume

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