• Master's Degree Computer science or related field and 5 year relevant experience Req Or
• Bachelor's Degree Computer science or related field and 6 years relevant experience Req
• Equivalent combination of education, training and experience Req
• Knowledge of statistics, programming and/or clinical drug development

• Collaborates effectively with the clinical team, biomarker scientists, and the study statistical programming team to meet biomarker analysis deliverables and timelines.
• Possesses knowledge of clinical trial study design and various biomarker assay types, including but not limited to immunohistochemistry, cell phenotype, and next-generation sequencing.
• Demonstrates knowledge of CDISC standards for SDTM, ADaM, and has experience with submissions to regulatory agencies.
• Proficient in SAS programming, with an in-depth understanding of SAS GTL.
• Proficient in R programming, using data science library packages such as tidyverse, pharmaverse, and shiny.
• Demonstrates statistical knowledge, interprets complex datasets, and applies modeling methods in both SAS and R languages.
• Familiar with Microsoft Excel, Microsoft Word, and Adobe PDF.
• Exhibits excellent verbal and written communication skills, as well as strong interpersonal skills.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com