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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 Responsibilities Author, QC, and implement Statistical Analysis Plans (SAPs) with minimal oversight Develop and validate SAS and/or R programs for tables, listings, and figures (TLFs), including reusable macros Perform QC/peer review and validation of statistical programs Produce statistical study reports and communicate results to clinical and cross-functional teams Review and contribute to statistical sections of study protocols Ensure compliance with CDISC SDTM and ADaM standards Must Have Minimum 5 years of experience in biostatistics/statistics, with substantial experience in pharmaceutical or biotech clinical development Strong programming skills in SAS and/or R Expertise in QC and validation processes Solid understanding of clinical trial design and analysis methods Nice to Have PhD in Biostatistics or Statistics Experience in CNS therapeutic area Knowledge of adaptive designs and real-world evidence analyses Excellent communication skills Education & Experience PhD: Minimum 3 years of relevant experience Master’s: Minimum 5 years of relevant experience 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 #J-18808-Ljbffr
