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