Biostatistical Programming Associate
Based in India
Core
Perform hands-on statistical programming to support data analysis for Phase 1-4 clinical studies and regulatory submissions.
Role type
Biostatistical Programming Associate
Builds
Clinical trial analysis datasets (SDTM, ADaM) and tables, listings, and figures for safety and efficacy.
Domain
Biotechnology / Clinical Development
Required skills
SAS, R, CDISC SDTM standards, CDISC ADaM standards, CDISC Define standards, data quality check tools, clinical trial data manipulation
Preferred skills
Python, automation platforms, regulatory submission experience
Responsibilities
Create and validate SDTM and ADaM datasets; generate tables, listings, and figures; maintain tracking and validation documentation; collaborate with cross-functional teams to validate data quality programs.
Seniority
Mid-level, hands-on IC
