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Job description
The Senior Statistical Programmer is responsible for all statistical programming aspects of assigned studies or project-level activities. The position is a key contributor with biostatistics in ensuring that pharmaceutical drug-development plans in Novartis are executed efficiently with timely and high quality deliverables.
Lead statistical programming activities for Phase I–IV studies and project‐level tasks, ensuring high‐quality planning and execution. Develop and validate high‐quality analysis datasets and outputs (CSRs, regulatory submissions, safety reports, publications) in compliance with CDISC and internal standards.
This role requires expertise in R or SAS, with at least 5 years of experience in clinical trials and programming. The ideal candidate will have experience in leading programming teams and contributing to process optimization initiatives.
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Healthcare • Manufacturing
Novartis Oncology, a division of Novartis, leverages science‑based innovation to discover, develop, and deliver breakthrough cancer therapies. The unit’s portfolio addresses more than 25 oncology indications across five key areas—breast, lung, melanoma, kidney, and hematologic cancers—and currently has around 30 investigational compounds in development. Committed to expanding patient access worldwide, Novartis Oncology integrates cutting‑edge research, immuno‑oncology, and rigorous quality standards to bring new treatments to market, offering a dynamic environment for professionals dedicated to advancing oncology care.