Associate Director, Biostatistics jobs in United States
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Alumis · 2 days ago

Associate Director, Biostatistics

Alumis Inc. is a precision medicines company dedicated to transforming the lives of patients with autoimmune diseases. They are seeking an Associate Director of Biostatistics to provide statistical expertise and operational support for clinical programs, contributing to study design and analysis while collaborating with cross-functional teams.

BiotechnologyHealth CareLife ScienceMedicalPrecision Medicine

Responsibilities

Contribute to the statistical design and analysis of early and late phase clinical studies
Apply advanced statistical methods and data visualization skills to clinical trial data summaries and interpretations such as integrated safety and efficacy analyses for regulatory submissions
Serve as the biostatistics representative on cross-functional teams, ensuring alignment of statistical approaches with study and program objectives
Provide input on study design, endpoint selection, and sample size planning
Draft statistical analysis plans (SAPs) and support interpretation of results
Ensure the quality and accuracy of statistical deliverables by independently generating the statistical deliverables and/or independently reviewing and validating the statistical deliverables generated by either CRO or internal statistical programming team
Manage CROs and mentor junior staff or contractors as appropriate

Qualification

Ph.D. in BiostatisticsStatistical programming SASStatistical programming RClinical trial designRegulatory submissions experienceExperience in immunologyManaging CROsAnalytical thinkingCommunication skillsOrganizational skillsCollaborative mindset

Required

Ph.D. in Biostatistics with 6+ years of relevant industry experience, or Master's with 8+ years
Significant experience serving as a study statistician on global Phase III clinical trials, ideally in immunology or immune-mediated diseases
Demonstrated track record of supporting regulatory submissions (NDA/BLA/MAA), including integrated safety/efficacy analyses
Hands-on experience working in a biotechnology or pharmaceutical company environment (not only CRO, Site, or Academic)
Proven ability to manage CROs and statistical programming teams in a sponsor setting
Strong foundation in clinical trial design, statistical analysis, and regulatory guidelines
Proficiency in statistical programming (SAS and R)
Demonstrated ability to manage multiple priorities and work cross-functionally
Experience with both early-stage and late-phase clinical trials
Strong analytical thinking and attention to detail
Excellent verbal and written communication skills
Ability to work independently in a fast-paced, regulated environment
Ability to manage deliverables with competing priorities and influence others effectively
Strong organizational skills, with the ability to manage workflows and activities to meet department timelines
Collaborative mindset and ability to influence without authority

Preferred

Experience in publication work and/or analysis of real-world data

Benefits

Health insurance premiums paid at 90% for employee, 80% for dependents
Free access to Genentech Bus & Ferry Share program
$100 monthly cell phone stipend
Unlimited PTO for Exempt employees
Free onsite gym and a kitchen stocked with yummy snacks and drinks!

Company

Alumis

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Alumis is a precision medicine company focused on the discovery, development and treatment of autoimmune disorders.

Funding

Current Stage
Public Company
Total Funding
$572.09M
Key Investors
Foresite CapitalMatrix Capital Management
2025-11-19Secondary Market· $3.09M
2024-07-23Post Ipo Equity· $40M
2024-06-28IPO

Leadership Team

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Martin Babler
Chairman, President and CEO
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Ken A Brameld
Fellow, Head of Discovery
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Company data provided by crunchbase