remote
Senior Statistical Programmer - Kodiak Sciences Inc.
Software Engineer
Senior Statistical Programmer with expertise in SAS, R, and CDISC standards to develop and validate clinical trial datasets, statistical analysis programs, and deliver high‑quality deliverables for ophthalmology drug development.
About the role
Key Responsibilities
- Develop, validate, and maintain SAS and R programs for creating analysis datasets (ADaM) and tables, listings, and figures (TLFs) in compliance with CDISC standards.
- Collaborate with biostatisticians, data managers, and clinical teams to translate statistical analysis plans into executable code.
- Perform data review, quality checks, and debugging to ensure accuracy and regulatory compliance of clinical study deliverables.
- Automate routine programming tasks using Python or SQL to improve efficiency and reproducibility.
- Support multiple concurrent ophthalmology studies, providing timely programming deliverables for interim and final analyses.
Requirements
- 5+ years of experience in statistical programming within the pharmaceutical or biotech industry.
- Proficiency in SAS (Base, Macro, PROC REPORT) and strong knowledge of CDISC SDTM/ADaM standards.
- Hands‑on experience with R and/or Python for data manipulation and statistical analysis.
- Solid understanding of clinical trial processes, regulatory requirements, and data management workflows.
- Excellent problem‑solving, communication, and teamwork skills.