Location: Mexico, Argentina or Brazil (Remote – must be available to work Eastern or Central U.S. time zones) We are seeking an experienced Principal Statistician to join our BIOS team for one of our FSP clients. This advanced-level position requires strong expertise in biostatistics and programming, with a focus on clinical development in the pharmaceutical or biotech industry.Key ResponsibilitiesAuthor, QC, and implement Statistical Analysis Plans (SAPs) with minimal oversightDevelop and validate SAS and/or R programs for tables, listings, and figures (TLFs), including reusable macrosPerform QC/peer review and validation of statistical programsProduce statistical study reports and communicate results to clinical and cross-functional teamsReview and contribute to statistical sections of study protocolsEnsure compliance with CDISC SDTM and ADaM standardsMust HaveMinimum 5 years of experience in biostatistics/statistics, with substantial experience in pharmaceutical or biotech clinical developmentStrong programming skills in SAS and/or RExpertise in QC and validation processesSolid understanding of clinical trial design and analysis methodsNice to HavePhD in Biostatistics or StatisticsExperience in CNS therapeutic areaKnowledge of adaptive designs and real-world evidence analysesExcellent communication skillsEducation & ExperiencePhD: Minimum 3 years of relevant experienceMaster's: Minimum 5 years of relevant experienceIQVIA 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