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Associate Director, Statistical Programming
Job Summary
A company is looking for an Associate Director, Evidence Generation Statistical Programming.
Key Responsibilities
- Provide statistical programming support for regulatory submissions and oversee programming technical decisions
- Develop programming standards and templates to enhance efficiency and quality in clinical trial data analysis
- Evaluate and improve the computing environment system for programming and analysis efficiency
Required Qualifications
- Bachelor's Degree in a science or technical field preferred; 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 CDISC SDTM and ADaM, with extensive implementation experience in clinical trials analysis preferred
- Strong understanding of statistical concepts related to clinical trials preferred
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