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r sas cdisc sdtm oncology📋 Description
- Lead programming activities for oncology clinical trials across multiple studies.
- Develop, validate, and maintain SDTM and ADaM datasets per CDISC guidelines.
- Oversee production of Tables, Listings, and Figures (TLFs) for study reporting.
- Act as programming lead for assigned studies, managing timelines and deliverables.
- Coordinate with CROs and external vendors to ensure compliance and quality.
- Provide SAS programming expertise to support data derivations and analyses.
🎯 Requirements
- 8-12+ years of statistical programming experience in pharma/biotech or CRO.
- Expert-level proficiency in SAS.
- Strong knowledge of CDISC SDTM and ADaM standards.
- Significant oncology clinical trials experience.
- Experience supporting regulatory submissions (FDA/EMA/PMDA).
- Bachelor's or Master's degree in Statistics, CS, Mathematics, Life Sciences, or related field.
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