Statistical programmer - junior level

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 ADa M 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 adherence to SOPs, Gx P guidelines, and regulatory standards
- Maintain complete programming documentation and version control
- Collaborate with biostatistics, data management, and clinical teams
Required Skil...