About the role

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 (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

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JOB OVERVIEW

Experience level

Senior

Location

Denver, CO

Occupation

Biostatisticians

Industry

Other Scientific and Technical Consulting Services

Posted

2 days ago

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