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Associate Director, SDTM Programming
Job Summary
A company is looking for an Associate Director - SDTM programming.
Key Responsibilities
- Support project leads on outsourced projects and ensure effective vendor programming implementation for regulatory submissions
- Provide hands-on statistical programming support for regulatory submissions and develop submission data packages
- Develop and maintain programming standards and tools to improve efficiency and quality in clinical trial data analysis
Required Qualifications
- Bachelor's Degree in a science or technical field preferred; 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 and CDISC SDTM/ADaM implementation
- Understanding of statistical concepts and methods used in clinical trials
- Knowledge of drug development phases and experience with SAS macro/system utility development preferred
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COMPLETE JOB DESCRIPTION
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