Principal Biostatistician
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Job Description
Principal Statistician responsible for statistical analysis and programming in clinical development for pharmaceuticals. Collaborating with cross-functional teams and ensuring compliance with industry standards.
Responsibilities:
- Author, QC, and implement Statistical Analysis Plans (SAPs)
- Develop and validate SAS and/or R programs for tables, listings, and figures (TLFs)
- 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
Requirements:
- Minimum 5 years of experience in biostatistics/statistics
- 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 (nice to have)
- Experience in CNS therapeutic area (nice to have)
Benefits:
- Health insurance
- Professional development
- Paid time off
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