Assistant Statistical Programming Specialist

Role Summary

We are seeking a Statistical Programmer with 1–2 years of experience to support clinical trial programming activities within a CRO environment. The role focuses on developing high-quality statistical outputs in compliance with CDISC standards, SOPs, and regulatory requirements, while working closely with biostatisticians and cross-functional teams.

Key Responsibilities

• Develop and maintain SAS programs for clinical trial data analysis
• Create and validate SDTM and ADaM datasets in accordance with CDISC standards
• Generate Tables, Listings, and Figures (TLFs) for clinical study deliverables
• Perform QC and independent validation of datasets and outputs
• Support interim, final analyses, and Clinical Study Reports (CSRs)
• Ensure adheren...