Conduct statistical analyses using software such as SAS.Write and maintain programs for data manipulation and analysis.Responsible for the quality control of statistical programming deliverables, including datasets, tables,listings, and figures.Verifying the accuracy and consistency of data and statistical analyses, ensuring compliance withregulatory requirements, and maintaining high standards of data integrity.Maintain comprehensive documentation of QC processes… Show more Conduct statistical analyses using software such as SAS.Write and maintain programs for data manipulation and analysis.Responsible for the quality control of statistical programming deliverables, including datasets, tables,listings, and figures.Verifying the accuracy and consistency of data and statistical analyses, ensuring compliance withregulatory requirements, and maintaining high standards of data integrity.Maintain comprehensive documentation of QC processes, findings, and resolutions.Ensure that all QC activities comply with relevant regulatory guidelines (e.g. FDA) and industrystandards (e.g. CDISC).Work closely with statistical programmers, biostatisticians, and data management teams to resolveany issues identified during the QC process. Show less

Conduct statistical analyses using software such as SAS.Write and maintain programs for data manipulation and analysis.Create and validate output formats in compliance with regulatory standards (e.g. CDISC, SDTM, ADaM).Generate tables, listings, and figures for clinical study reports, publications, and presentations.Ensure code is efficient, reliable, and well-documented.Ensure compliance with regulatory requirements and guidelines.