Principal Biostatistician
IQVIA
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇲🇽 Mexico
Visit company websiteJob Level
Mid-LevelSenior
About the role
- 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
Requirements
- 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
- PhD in Biostatistics or Statistics preferred
- Experience in CNS therapeutic area preferred
- Knowledge of adaptive designs and real-world evidence analyses preferred
- Excellent communication skills
Benefits
- Health insurance
- Flexible working arrangements
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
SASRStatistical Analysis Plans (SAPs)QC/peer reviewvalidation processesclinical trial designadaptive designsreal-world evidence analysesstatistical study reportsreusable macros
Soft skills
communication skills
Certifications
PhD in BiostatisticsPhD in Statistics