Principal Biostatistician
Posted 102ds ago
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Job Description
Principal Statistician role focused on biostatistics and programming for clinical development in pharma. Joining BIOS team to manage statistical analysis plans and communicate findings.
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
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













