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Associate Director, Statistical Programming
A company is looking for an Associate Director, Evidence Generation Statistical Programming. Key Responsibilities Provide statistical programming support for regulatory submissions and ensure compliance with CDISC standards Develop and maintain programming standards, templates, and tools to enhance efficiency and quality in data analysis Evaluate and improve the computing environment for programming and analysis, addressing system issues and upgrades Required Qualifications Bachelor's Degree in a science or technical field; Master's Degree preferred 10+ years of experience in the pharmaceutical industry or CROs supporting statistical analysis of clinical trials with a Bachelor's degree; 7+ years with a Master's degree Experience in SAS macro and/or system utility development preferred Advanced knowledge of SAS programming, CDISC SDTM, and ADaM in clinical trials Understanding of statistical concepts and methodologies in clinical trial analysis
A company is looking for an Associate Director, Evidence Generation Statistical Programming.
Key Responsibilities
Provide statistical programming support for regulatory submissions and ensure compliance with CDISC standards
Develop and maintain programming standards, templates, and tools to enhance efficiency and quality in data analysis
Evaluate and improve the computing environment for programming and analysis, addressing system issues and upgrades
Required Qualifications
Bachelor's Degree in a science or technical field; Master's Degree preferred
10+ years of experience in the pharmaceutical industry or CROs supporting statistical analysis of clinical trials with a Bachelor's degree; 7+ years with a Master's degree
Experience in SAS macro and/or system utility development preferred
Advanced knowledge of SAS programming, CDISC SDTM, and ADaM in clinical trials
Understanding of statistical concepts and methodologies in clinical trial analysis