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Job Description & How to Apply Below
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 adherence to SOPs, GxP guidelines, and regulatory standards
Maintain complete programming documentation and version control
Collaborate with biostatistics, data management, and clinical teams
Required Skills & Experience
1–2 years of hands-on experience in statistical programming within a CRO
Strong proficiency in SAS (Base SAS, Macros)
Working knowledge of CDISC (SDTM, ADaM)
Understanding of the clinical trial lifecycle
Experience working in a regulated, deadline-driven environment
Good analytical , problem-solving, and communication skills
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