Contract Statistical Programmer US or CanadaGlobal Pharma (FSP) Remote / US or Canada 12-month contract Considering applying for this job Do not delay, scroll down and make your application as soon as possible to avoid missing out. We are supporting a global pharmaceutical organisation in the search for an experienced Statistical Programmer to join a specialist biometrics function on a contract basis. This role sits within the Independent Safety and Statistical Analysis Team - a specialist group responsible for independent oversight of statistical and safety analyses across clinical development programmes.
What you'll be doing:
  • Delivering statistical programming support for clinical trial analysis and reporting activities
  • Developing and validating datasets, tables, listings, and figures (TLFs)
  • Supporting independent safety and statistical analysis workstreams within iSATCollaborating with biostatistics and clinical teams to ensure high-quality deliverables
  • Contributing to programming standards, QC processes, and regulatory compliance activities
What we're looking for: Strong hands-on SAS programming experience in a clinical or pharma environmentR programming experience within clinical research or pharmaceutical settings xhqgsiq Experience supporting clinical trial analysis within biotech, pharma, or CRO settings Solid understanding of clinical data standards and reporting requirements
Nice to have:
  • Experience supporting safety analyses or independent statistical review activities
  • Familiarity with regulatory submission environments
  • Previous exposure to global clinical development teams

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Level

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Posted

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