Contractor, Biostatistician

Position Description:

We are seeking an experienced Contractor, Biostatistician to support Clinical Development and Medical Affairs. The role will support data analysis strategy and execution including publication based on clinical trials, external comparator analyses, and evidence generation strategies to support post‑marketing, payer, and hypothesis generation analysis. This role will also provide statistical consultation to the analysis of real-world data. This position requires close collaboration with cross-functional teams including Clinical Development, Medical, HEOR, and Commercial.

Responsibilities and Duties:

• Partner with medical for publication strategies
• Provide statistical expertise in analyses using external control and/or synthetic control, meta-analyses, and causal inference analyses, e.g. propensity score matching method
• Contribute to manuscripts, abstracts and presentations
• Write and/or review statistical analysis plans
• Work with statistical programmers to conduct ad hoc analyses; Conduct quality review of statistical analyses
• Perform statistical programming for advanced statistical methodologies and help statistical programmers QC their programs
• Develop TLF shells and review programming specs
• Review protocols for real world evidence studies
• Review relevant medical literature

Minimum Requirements:

Experience: 

• S., Biostatistics or Ph.D. in Biostatistics or equivalent with at least 5 years of pharmaceutical, biotechnology, or equivalent experience.

Other:

• Good understanding of meta-analyses and causal inference methodologies
• Prior experience working 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
• Understand good clinical practice guidelines
• Good statistical programming skills using relevant statistical software
• Familiarity with regulatory guidance on RWE and HTA requirements
• Oncology experience preferred

Location: Syndax’s corporate office is in New York, NY.

This is a remote opportunity.

About Syndax:
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company’s pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn.

Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

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