Contract Statistical Programmer – Independent Safety Analyses

Warman O'Brien; United States; Sur place; USD 90 000 - 130 000; Plein temps

Résumé du poste

Warman O'Brien is seeking an experienced Statistical Programmer to join a global pharmaceutical organisation on a contract basis. You will deliver programming support for trial analyses, develop TLFs, and ensure data quality across iSAT initiatives, collaborating with biostatistics and clinical teams to maintain regulatory-compliant processes.

Ideal candidates have hands-on SAS experience in pharma, plus R skills, and a strong understanding of clinical data standards and reporting requirements.

Qualifications

• 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.

Responsabilités

• 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.

Outils

SAS

R

Description du poste

Warman O'Brien is seeking an experienced Statistical Programmer to join a global pharmaceutical organisation on a contract basis. You will deliver programming support for trial analyses, develop TLFs, and ensure data quality across iSAT initiatives, collaborating with biostatistics and clinical teams to maintain regulatory-compliant processes.

Ideal candidates have hands-on SAS experience in pharma, plus R skills, and a strong understanding of clinical data standards and reporting requirements.