Lead programming activities for oncology clinical trials across multiple studies.
Develop, validate, and maintain SDTM and ADaM datasets per CDISC.
Oversee production of Tables, Listings, and Figures for reports and submissions.
Provide SAS programming expertise for complex data derivations and analyses.
Review and ensure traceability, consistency, and quality of all deliverables.
Manage timelines and deliverables as programming lead.

🎯 Requirements

8–12+ years of statistical programming experience in pharma/biotech or CRO.
Expert SAS; working knowledge of R.
CDISC SDTM and ADaM standards expertise.
Oncology clinical trials experience (hematologic or solid tumors).
Bachelor's or Master's degree in Statistics, CS, Mathematics, Life Sciences, or related field.
Experience leading studies; coordinating with CROs/vendors and regulatory submissions.

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