Develop, maintain and validate SAS programs for clinical trial data.
Create and validate analysis datasets, tables, listings and figures (TLFs).
Support the development of SDTM and ADaM datasets in accordance with CDISC standards.
Perform statistical programming for safety and efficacy analyses.
Review programming specifications and statistical analysis plans.
Perform quality control checks and investigate discrepancies.
Develop and maintain SAS macros and reusable programming utilities.
Ensure programming outputs are accurate, reproducible and properly documented.
Support data review and reconciliation activities.
Collaborate with biostatisticians, data managers and clinical project teams.
Contribute to clinical study reports and regulatory submission deliverables where required.
Follow company standard operating procedures, programming standards and quality processes.
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Contact Details:
CHANDRAWAR IT TECHNOLOGIES PVT LTD Recruitment Team
