Contract Statistical Programmer
Contract Statistical Programmer US or CanadaGlobal Pharma (FSP) Remote / US or Canada 12-month contract 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 (iSAT) - 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
- 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