Job Description :
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following.

  • Writing specifications for SAS programs/macros for study specific analyses or at the standard level
  • Developing, maintaining and validating SAS programs/macros forstudy specific analyses or at the standard level
  • Plans and participates in programming/QC activities at a study- or standard level to deliver all data analysis outputs
  • Develops the tables, figures and listings (TFL)
  • Reviews and ensures adherence to standards at the study or standard level (e.g., especially in the area of Analysis Data Model (ADaM) and Study Data Tabulation Model (SDTM) datasets, derivation, output definition and implementation).
  • Author or co-author of programming and database specifications and documentation
  • May represent the programming function on the study team.

We are looking for an experience individual and if you have these skills, we would like to speak to you.

  • Experience in SAS programming (including SQL and SAS macro language)
  • Experience in CDISC
  • Ability to design, test and maintain programs.
  • Ability to create programs for multiple use
  • Understanding of clinical trial process.
  • Basic knowledge of applied statistics is an asset
  • Knowledge in CDISC format (SDTM andADaM)

Our goalis to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing.
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