Source description
About the role
Perform statistical analysis for clinical trial data. Develop Statistical Analysis Plans (SAP). Generate Tables, Listings & Figures (TLFs). Perform SAS programming and data validation. Work with CDISC SDTM & ADaM standards. Support Clinical Study Reports (CSR). Conduct survival and regression analysis. Review and validate clinical trial datasets. Collaborate with Clinical, Data Management and Regulatory teams. Ensure compliance with ICH-GCP, ICH E9 and USFDA guidelines.
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