Statistical Programming Associate Director (cvrm)

Trzdev36

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.
  • Lead and direct project delivery while ensuring high quality and compliance to standards.
  • Contribute to a diverse and collaborative work environment that fosters innovation and growth.

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 related field
  • Proficient in SAS or R programming
  • Experience in clinical drug development

Work Rights

Not specified

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