Contractor, Biostatistician
Syndax Pharmaceuticals
August 08, 2026
Remote
United States
Clinical Research and Development
Position: Contractor, Biostatistician (Remote)
Responsibilities:
- Partner with Medical on publication strategies
- Provide statistical expertise for external control/synthetic control analyses, meta-analyses, and causal inference (e.g., propensity score matching)
- Contribute to manuscripts, abstracts, and presentations
- Write and/or review statistical analysis plans (SAPs)
- Collaborate with statistical programmers on ad hoc analyses; conduct QC of statistical analyses
- Perform statistical programming for advanced methods and help QC programmers’ code
- Develop TLF shells and review programming specifications
- Review protocols for real-world evidence (RWE) studies
- Review relevant medical literature
Minimum Requirements:
- MS in Biostatistics or Ph.D. in Biostatistics (or equivalent) with at least 5 years of pharmaceutical/biotechnology (or equivalent) experience
Required/Preferred Skills:
- Strong understanding of meta-analyses and causal inference
- Prior experience with Medical Affairs and Commercial
- Strong statistical reasoning and problem-solving
- Ability to communicate complex methods to non-statistical stakeholders
- High attention to data quality and methodological rigor
- Ability to work independently in a fast-paced cross-functional environment
- Knowledge of good clinical practice guidelines
- Strong statistical programming skills using relevant software
- Familiarity with regulatory guidance on RWE and HTA requirements
- Oncology experience preferred
Responsibilities:
- Partner with Medical on publication strategies
- Provide statistical expertise for external control/synthetic control analyses, meta-analyses, and causal inference (e.g., propensity score matching)
- Contribute to manuscripts, abstracts, and presentations
- Write and/or review statistical analysis plans (SAPs)
- Collaborate with statistical programmers on ad hoc analyses; conduct QC of statistical analyses
- Perform statistical programming for advanced methods and help QC programmers’ code
- Develop TLF shells and review programming specifications
- Review protocols for real-world evidence (RWE) studies
- Review relevant medical literature
Minimum Requirements:
- MS in Biostatistics or Ph.D. in Biostatistics (or equivalent) with at least 5 years of pharmaceutical/biotechnology (or equivalent) experience
Required/Preferred Skills:
- Strong understanding of meta-analyses and causal inference
- Prior experience with Medical Affairs and Commercial
- Strong statistical reasoning and problem-solving
- Ability to communicate complex methods to non-statistical stakeholders
- High attention to data quality and methodological rigor
- Ability to work independently in a fast-paced cross-functional environment
- Knowledge of good clinical practice guidelines
- Strong statistical programming skills using relevant software
- Familiarity with regulatory guidance on RWE and HTA requirements
- Oncology experience preferred