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 https://jobs.iqvia.com
#J-18808-Ljbffr