Contract Statistical Programmer

Warman O'Brien; United States; On-site; USD 90,000 - 140,000; Full time

Job summary

Warman O'Brien is seeking an experienced Statistical Programmer to join a global pharmaceutical organisation on a contract basis. The role sits within the Independent Safety and Statistical Analysis Team (iSAT), providing independent oversight of statistical and safety analyses across clinical development programmes.

You will deliver programming support for trial analyses, develop and validate datasets, tables, listings, and figures (TLFs), and collaborate with biostatistics and clinical teams

Qualifications

• Strong hands‑on SAS programming experience in clinical or pharma environments.
• R programming within clinical research or pharmaceutical settings.
• Experience supporting clinical trial analysis in biotech, pharma, or CRO settings.

Responsibilities

• Deliver 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

Skills

SAS programming

R programming

Clinical trial analysis

Job description

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 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