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Director Statistical Analysis Jobs (NOW HIRING)

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$150 - $200/hr

Associate Director, Statistical Programming The Associate Director, Statistical Programming will ... Lead and perform the development and validation of analysis datasets and reporting outputs in ...

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As of Sep 9, 2026, the average yearly pay for director statistical analysis in the United States is $280,147.00, according to ZipRecruiter salary data. Most workers in this role earn between $260,500.00 and $322,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Director Statistical Analysis job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, 13% Part Time, and 4% Contract. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $280,147 per year, or $134.7 per hour.

Associate Director, Statistical Programming

Burlington, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$200 - $250/hr

Other

Posted 10 days ago

Job description

Position Summary

MBX is seeking an Associate Director, Statistical Programming to lead and contribute to statistical programming and analysis of clinical trial data.

What You’ll Do
  • Oversee and execute statistical programming deliverables for planned analyses (study monitoring, data reviews, clinical study reports, data integrations, regulatory query responses) across compounds and studies.
  • Lead global submission activities as a programming functional/technical expert; ensure deliverables meet timelines, quality, and regulatory expectations (ICH/FDA/EMA).
  • Manage CROs/contractors to ensure compliant, high-quality deliverables within timeline and budget.
  • Develop and validate reproducible, well-documented statistical programs for integrated scientific reports, aligned to protocols and Statistical Analysis Plans (SAPs) and regulatory conventions.
  • Maintain and enhance the internal SAS macro library and database.
  • Provide input to SAPs, publications, scientific presentations, regulatory submissions, and promotional materials.
  • Review CRFs/CRF annotations, SAPs, TLF shells and outputs, and dataset specifications (SDTM/ADaM).
  • Lead statistical programming within study teams; communicate statistical/programming issues to development teams.
  • Contribute to programming standards, macros, SOPs, and process improvements.
  • Other responsibilities as assigned.
What You Bring
  • 8+ years statistical programming experience in biotech/pharma (preferred: endocrine/metabolic disorders).
  • Advanced degree (PhD/MS/etc.) preferred.
  • Proficient in SAS (Base SAS, SAS/Stat, SAS/Graph, macros, ODS) and solid understanding of database systems.
  • R and Python experience preferred.
  • CDISC experience (SDTM, ADaM, define.xml) and eCTD/eSub submissions.
  • Ability to lead programming and oversee CRO deliverables.
  • Strong analytical, organizational, communication skills; manage multiple priorities.
Travel & In Office Presence
  • Periodic travel and hybrid work schedule based on business needs/office practices.
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