Senior Statistical Programmer

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