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Senior Statistical Programmer Consultant
A company is looking for a Senior Statistical Programmer, Early Stage Development and PK/PD Modeling and Simulation Consultant. 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 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
A company is looking for a Senior Statistical Programmer, Early Stage Development and PK/PD Modeling and Simulation Consultant.
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 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