Senior Statistical Programmer
A company is looking for a Senior Statistical Programmer, PK/PD Modeling and Simulation Consultant.
Key Responsibilities
Provide statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders
Gather and interpret user requirements, create modeling-ready datasets, and produce tables and graphics for study reports
Lead data stewardship and collaborate with modelers, statisticians, and project stakeholders
Required Qualifications and Education
BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, or related field plus 5-9 years of SAS programming experience in a clinical trial environment
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, or related field plus 3-7 years of SAS programming experience in a clinical trial environment
Significant expertise in SAS and clinical trial programming, including data steps, procedures, and SAS/MACRO
Ability to comprehend analysis plans and implement statistical methods not available through commercial software
Experience in efficiently manipulating clinical trial datasets, including complex data preprocessing and pharmacokinetic data
A company is looking for a Senior Statistical Programmer, PK/PD Modeling and Simulation Consultant.
Key Responsibilities
Provide statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders
Gather and interpret user requirements, create modeling-ready datasets, and produce tables and graphics for study reports
Lead data stewardship and collaborate with modelers, statisticians, and project stakeholders
Required Qualifications and Education
BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, or related field plus 5-9 years of SAS programming experience in a clinical trial environment
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, or related field plus 3-7 years of SAS programming experience in a clinical trial environment
Significant expertise in SAS and clinical trial programming, including data steps, procedures, and SAS/MACRO
Ability to comprehend analysis plans and implement statistical methods not available through commercial software
Experience in efficiently manipulating clinical trial datasets, including complex data preprocessing and pharmacokinetic data