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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 ensure compliance with CDISC standards
- Develop and maintain programming standards, templates, and tools to enhance efficiency and quality
- Evaluate and improve the computing environment for statistical programming and analysis
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 in statistical analysis of clinical trials with a Bachelor's degree; 7+ years with a Master's degree
- Experience with SAS macro and system utility development preferred
- Advanced knowledge of CDISC SDTM and ADaM standards and their implementation in clinical trials
- Strong understanding of statistical concepts and methods relevant to clinical trial analysis
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