Statistical Programming Associate Director (cvrm)

AstraZeneca

Warsaw, Poland
3d onsite
Sas programming
Clinical drug development knowledge
Cdisc standards implementation
Join a fast-paced and agile global team with direct strategic impact on drug development

Job Summary

  • Join a fast-paced and agile global team with direct strategic impact on drug development.
  • This role is a delivery-focused technical leadership position overseeing programming deliverables with quality and timeliness.
  • You will play a pivotal role in making a positive impact on changing patients’ lives through your work in Cardiovascular Renal Metabolism (CVRM) Biometrics.

Matching Summary

Join a fast-paced and agile global team with direct strategic impact on drug development.

Skills & Requirements

Must-have

  • SAS programming
  • clinical drug development knowledge
  • CDISC standards implementation
  • technical leadership
  • quality and timeliness focus

Nice-to-have

  • cross-functional team collaboration
  • process improvement initiatives
  • mentorship and training
  • external partner management

Key Requirements

  • Degree in Mathematics, Statistics, Computer Science, Life Science, or equivalent
  • Excellent programming skills in SAS (or R)
  • Thorough knowledge of clinical development process
  • Thorough knowledge of industry standards (CDISC)
  • Ability to manage risk in complicated or novel situations

Work Rights

Not specified

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