Senior Statistical Programmer

Job Description

Kindly share your updated resume to heena.gill@qvia.com Role & responsibilities Minimum 6+ Years of experience . Works collaboratively with clinical bioinformatics, biomarker scientists and study statistical programming team, to meet biomarker analysis deliverables and timelines Has knowledge of clinical trial study design and biomarker assay types, including but not limited to Immunohistochemistry, cell phenotype, next gene sequencing. Demonstrate knowledge of CDISC standards for SDTM, ADaM and submission experience to regulatory agencies. Demonstrates SAS programming proficiency, including in depth understanding of graphical template languages and using internal macros or writes SAS macros to automate study deliverables. Demonstrates R programming proficiency in using data science library packages including but not limited to tidyverse, pharmaverse and shiny. Demonstrate statistical knowledge, interpret complex dataset and modeling methods in both SAS and R languages. Must be familiar with Microsoft Excel, Microsoft Word, Adobe PDF. Role & responsibilities