Statistical Programming Associate Director (cvrm)

AstraZeneca

Warsaw, Poland
3d onsite
Excellent programming skills in sas
Thorough knowledge of clinical development process
Ability to manage risk in complicated situations
Join a fast-paced and agile global team at AstraZeneca CVRM to impact drug development

Job Summary

  • Join a fast-paced and agile global team at AstraZeneca CVRM to impact drug development.
  • This role involves leading statistical programming aspects and ensuring high-quality project deliverables.
  • You will contribute to continuous improvement and best practices within the programming discipline.

Matching Summary

Join a fast-paced and agile global team at AstraZeneca CVRM to impact drug development.

Skills & Requirements

Must-have

  • Excellent programming skills in SAS
  • Thorough knowledge of clinical development process
  • Ability to manage risk in complicated situations

Nice-to-have

  • Broad experience across multiple therapeutic areas
  • Experience in regulatory submissions
  • Proactive management of concurrent activities

Key Requirements

  • Degree in Mathematics, Statistics, or Life Science
  • Proficient in SAS or R programming
  • Current knowledge of industry standards (CDISC)

Work Rights

Not specified

Tailored Resume

Cover Letter