Contract Statistical Programmer
US or Canada
Global 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 - 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 iSAT
- Collaborating 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 environment
- R 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
Contract Statistical Programmer in United States at Warman O'Brien
This position is listed as contract and able to be worked remotely. It was posted 3 days ago.