Job Description
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
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