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Contractor, Biostatistician

Syndax Pharmaceuticals Inc - New York, NY

Posted Jun 4, 2026

Benefits

Parental leave
Not verified
Non-birth-parent leave
Not verified
Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
Not verified
Relocation assistance
Not verified
Childcare support
Not verified
Learning budget
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Verification
Not verified checked Jun 13, 2026
Salary
Not verified
401(k) match
Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)
$111,944 U.S. median for this role
Projected growth (BLS Employment Projections)
+13.7% - Much faster than average

Matched to SOC 15-1252 - Data and ML aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function
Data From the posting source checked Jun 20, 2026
Seniority
Mid From the posting source checked Jun 20, 2026

Schedule

Shift type
Not verified
Weekend work
Not verified

Company

Company stage
Public-company From the posting source checked Jun 20, 2026
Equity
Offered Verified - SEC 10-K source checked Jun 20, 2026

Application

Cover letter
Not verified
Assessment
Not verified
Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

Contractor, Biostatistician New York, NY Position Description: We are seeking an experienced Contract Biostatistician to support Medical Affairs and Real‑World Evidence (RWE) activities. The role will provide statistical leadership in the design, analysis, and interpretation of RWE/observational studies, external comparator analyses, and evidence generation strategies to support post‑marketing, payer, and hypothesis generation analysis. This position requires close collaboration with cross-functional teams including Medical, HEOR, Clinical Development, and Commercial. Responsibilities and Duties: - Partner with medical for publication strategies, HEOR or economic modeling inputs - 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 - Collaborate with HEOR to align analyses with HTA agency expectations - Review protocols for real world evidence studies - 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 - Review relevant medical literature - Write statistical analysis plans - Develop TLF shells and review programming specs Minimum Requirements: Experience : - M.S., Biostatistics or Ph.D. in Biostatistics or equivalent with at least 5 years of pharmaceutical, biotechnology, or equivalent experience. Other: - Prior experience working with medical affairs and commercial - Good understanding of meta-analyses and causal inference methodologies - Familiarity with regulatory guidance on RWE and HTA requirements - Strong statistical reasoning and problem-solving - Ability to communicate complex methods to non-statistical stakeholders - High

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