Statistical Programmer

ICON · Tokyo, Japan +1 more

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Role summary

Statistical programmer needed to develop and validate SAS, R, or Python programs supporting clinical trial analysis and reporting at a contract research organization. Role involves collaborating with biostatisticians, ensuring regulatory compliance, and preparing statistical documentation in a sponsor-dedicated model.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-06 (originally posted 2026-10-05). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Bachelor's degree in statistics, computer science, mathematics, or related field
Proven clinical research statistical programming experience with strong methodological knowledge
Proficiency in SAS, R, Python, or similar programming languages
Experience with clinical data management systems
Strong analytical, problem-solving, and attention-to-detail skills
Excellent communication ability for technical and non-technical audiences
Legal right to work in Japan

What you'll be doing

Develop, validate, and maintain statistical programs for data manipulation, analysis, and reporting
Collaborate with biostatisticians and clinical teams to understand requirements and implement analyses accurately
Prepare and review statistical analysis plans and programming specifications for regulatory standards
Ensure data integrity and compliance with ICH/GCP guidelines throughout programming
Contribute to clinical study reports and regulatory documentation preparation

Privacy & handoff

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Date posted1 day ago

Last source checkToday

Salary listedNeeds clarity

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