Senior Statistical Programmer Consultant

Job Summary

A company is looking for a Senior Statistical Programmer, Early Stage Development and PK/PD Modeling and Simulation Consultant (Hybrid at PA/NJ).

Key Responsibilities

• Prepare compliant programming code for regulatory submissions including analysis/modeling datasets, tables, listings, figures, and associated documentation
• Ensure programmatic traceability from data source to analysis/modeling result
• Support the development of programming standards to enable efficient and high-quality production of programming deliverables

Required Qualifications, Training, and Education

• BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, or related field plus 5 years SAS programming experience in a clinical trial environment, or MS in the same fields plus 3 years SAS programming experience
• Programming expertise with clinical endpoint data and pharmacokinetic data
• Experience in CDISC SDTM and ADaM standards
• Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH
• Ability to comprehend analysis plans and implement statistical methods not currently available through commercial software packages