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Associate Director of SDTM Programming
Job Summary
A company is looking for an Associate Director - SDTM programming.
Key Responsibilities
- Provide statistical programming technical support and oversight for outsourced projects, ensuring compliance with regulatory submission standards
- Develop programming standards and templates for datasets and TFLs to enhance efficiency and quality in clinical trial data analysis
- Evaluate and enhance the computing environment system, identifying issues and leading improvements for programming efficiency
Required Qualifications
- Bachelor's Degree in a science or technical field; Master's Degree preferred
- 10 or more years of experience in the pharmaceutical industry or CROs supporting statistical analysis of clinical trials
- Advanced working knowledge of SAS programming language and CDISC SDTM/ADaM standards
- Solid understanding of statistical concepts and methodologies in clinical trials
- Knowledge of all phases of drug development and applied statistics
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COMPLETE JOB DESCRIPTION
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