Senior Clinical Statistical Programmer

Job Summary

A company is looking for a Senior Clinical Statistical Programmer to provide statistical programming support for early-phase clinical research.

Key Responsibilities

• Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages, statistical analyses, data listings, tables, and figures
• Perform peer QC, double programming, and validation functions for statistical outputs from studies
• Lead statistical programming activities on studies and deliverables, assisting management and biostatisticians with complex projects

Required Qualifications

• Minimum of a Bachelor's Degree in Statistics, Mathematical Science, Physics, or a Computing related field
• Minimum 3 years of hands-on statistical programming experience in a CRO or pharmaceutical clinical trials environment
• Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, and SAS/ODS
• Experience applying CDISC requirements to generate ADaM datasets and supporting documentation
• Familiarity with Pinnacle 21 validation and experience in early-phase clinical trials