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Associate Director, Statistical Programming
Job Summary
A company is looking for an Associate Director, Evidence Generation Statistical Programming.
Key Responsibilities
- Support project leads and provide statistical programming expertise for outsourced projects, ensuring quality and compliance of datasets and TLFs
- Deliver hands-on statistical programming support for regulatory submissions, including the development of submission data packages and analyses
- Develop and maintain programming standards and tools to enhance efficiency and quality in clinical trial data analysis
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 with a Bachelor's degree; 7+ years with a Master's degree
- Experience in SAS macro and system utility development preferred
- Advanced knowledge of CDISC SDTM and ADaM implementation in clinical trials
- Understanding of statistical concepts and drug development phases preferred
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COMPLETE JOB DESCRIPTION
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