Biostatistical Programming Associate
Amgen · Hyderabad, India
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Role summary
This role involves performing statistical programming activities to support clinical trial data analysis across phases 1–4 and regulatory submissions. Responsibilities include dataset creation and validation using SAS or R, generating tables and figures, and collaborating with global teams on data quality checks. The position requires a degree in biostatistics or related quantitative field with at least 3 years of clinical development experience.
Privacy & handoff
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