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Director Statistical Modeling Jobs (NOW HIRING)

Statistical programmers work collaboratively with internal colleagues and external vendors to ... Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding ...

Director of Biostatistics

Sunrise, FL ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Director of Biostatistics

Spokane, WA ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Director of Biostatistics

Midland, TX ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Director of Biostatistics

Carlsbad, CA ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Director of Biostatistics

San Mateo, CA ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Director of Biostatistics

Birmingham, AL ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Director of Biostatistics

Renton, WA ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Director of Biostatistics

Denton, TX ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Director of Biostatistics

Corona, CA ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Director of Biostatistics

Shreveport, LA ยท Remote

$60 - $65/hr

Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies ...

Showing results 41-60

Director Statistical Modeling information

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$153.5K

$280.1K

$344K

How much do director statistical modeling jobs pay per year?

As of Sep 10, 2026, the average yearly pay for director statistical modeling 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.

What states have the most Director Statistical Modeling jobs?

States with the most job openings for Director Statistical Modeling jobs include:

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Infographic showing various Director Statistical Modeling job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $280,147 per year, or $134.7 per hour.

Director, Biostatistics

Boston, MA โ€ข On-site

Monte Rosa Therapeutics, Inc
Biotechnology Research and Developmentย โ€ขย 11 - 50 employees

$230K - $265K/yr

Full-time

Re-posted 28 days ago


Job description

Overview
The Director of Biostatistics is a hands-on statistical leader responsible for the design, analysis, and interpretation of Phase 1-Phase 3 clinical trials with a primary focus on inflammation and oncology indications. This role combines scientific leadership with active execution and intensive CRO oversight, ensuring high-quality statistical deliverables across outsourced clinical studies.
The Director will work closely with Clinical Development and external partners to drive trial design, analysis strategies, and regulatory-ready outputs while remaining directly involved in study-level statistical activities.
Responsibilities
Statistical Leadership
  • Lead and personally contribute to statistical strategy and execution for Phase 1-3 clinical studies, including first-in-human, dose-escalation, proof-of-concept, and registrational trials in oncology and inflammatory diseases.
  • Provide direct input into trial design, endpoint selection, sample size justification, interim analyses, and adaptive strategies, particularly for early-stage development
  • Author, review, and approve:
    • Statistical sections of clinical protocols
    • Statistical Analysis Plans (SAPs)
    • Tables, listings, and figures (TLFs)
    • Clinical Study Reports (CSRs)

CRO Oversight & Execution
  • Serve as the primary statistical point of contact for CROs, providing close, day-to-day oversight of outsourced biostatistics and programming activities
  • Actively review CRO deliverables for scientific accuracy, consistency, and regulatory compliance, including datasets, analysis outputs, and reports
  • Ensure CROs adhere to agreed-upon timelines, quality standards, CDISC/CDASH conventions, and statistical methodologies
  • Lead CRO selection, scope definition, and ongoing performance management for biostatistics and programming services

Cross-Functional & Regulatory Engagement
  • Partner closely with Clinical Development to ensure statistical approaches align with program objectives and clinical strategy Finish
  • Provide statistical expertise for data monitoring committees, interim analyses, and data review meetings
  • Contribute directly to regulatory submissions, briefing documents, and responses to health authority questions
  • Represent biostatistics in cross-functional development teams and external regulatory interactions as needed

Operational Focus
  • Ensure the timely production and accuracy of all statistical analyses and integrated reports across assigned studies
  • Maintain consistency of statistical approaches across programs while remaining flexible to study-specific needs
  • Stay current on evolving statistical methodologies, regulatory expectations, and industry best practices relevant to oncology and inflammation trials

Statistical Programming Oversight
  • Direct and mentor statistical programmers to ensure accurate, timely, and compliant production of CDISC-compliant datasets (SDTM/ADaM), tables, listings, and figures (TLFs) for clinical study reports.
  • Translate Statistical Analysis Plans (SAPs) into clear, actionable programming specifications and define data structure requirements for external CRO partners or internal teams.
  • Ensure rigorous quality control (QC) and validation of analysis datasets and statistical outputs to meet FDA/EMA regulatory standards."
  • Collaborate with data management and clinical teams to resolve data issues and ensure consistency between clinical databases and statistical outputs.
  • Develop and implement efficient statistical programming workflows, macros, and best practices to improve productivity and compliance across multiple clinical trials

Qualifications
  • PhD in Biostatistics, Statistics, Mathematics, Computer Science, or related field
  • 15 +years of experience supporting clinical drug development, including Phase 1-Phase 3 trials and regulatory submissions
  • Demonstrated experience working in CRO-heavy models, with direct responsibility for reviewing and managing outsourced statistical work
  • Strong expertise in clinical trial statistics, regulatory standards (FDA, ICH), and industry best practices
  • Proficiency with SAS and other commonly used statistical software