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Senior / Principal - Statistical Programmer (SAS)

Lieu Varsovie, Voïvodie de Mazovie, Pologne Job ID R-142161 Date de publication 08/03/2022

The Senior / Principal Statistical Programmer is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes. This position requires technical skills and adequate industry knowledge to independently perform the programming tasks while using judgement about seeking guidance in complex situations. They can be responsible for supporting medium complex clinical study deliverables or part of project deliverables. It will act as a contributor on cross-functional teams, or a lead on small teams, to deliver continuous improvement

Typical Accountabilities

  • Collaborates with other team members to provide programming support to deliver technical programming and information components of a study or a project deliverable
  • Implements statistical programming aspects of the protocol or clinical development program
  • Ensures high quality is built into own deliverables and the deliverables of other programmers on the team
  • Programs independently with efficiency and quality
  • Writes specifications and oversees completeness of relevant documentation
  • Contributes to the development of best practices to improve quality, efficiency and effectiveness within function
  • Delivery of the Clinical Study Report (CSR), Study Data Tabulation Model (SDTM)/Analysis Data Model (ADaM) databases and Tables, Figures and Listings (TFL) outputs, following applicable data standards and regulations
  • Works cooperatively with study team members including but not limited to the statistician, lead programmer, data manager and study leader


  • Degree in Mathematics (i.e., Applied Math, Engineering, etc), Statistics, Computer Science, Life Science or equivalent
  • Extensive SAS programming knowledge and experience (SAS Base, Enterprise Guide, 4GL)
  • Accomplished programming skills including macro language
  • Intermediate knowledge of the clinical development process
  • Good knowledge of industry standards
  • Ability to apply programming knowledge to problem solving
  • Ability to manage relevant documentation


  • Familiarity with CDISC, Study Data Tabulation Model (SDTM), Analysis Data Model (ADaM) standards
  • Ability to proactively manage concurrent activities within their assigned study(ies) or project

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

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