Principal Biostatistician/Senior Principal Biostatistician

Precision For Medicine

Principal Biostatistician leading statistical initiatives for clinical development at Precision for Medicine. Engaging with clients on study design and statistical analysis for clinical trials.

Posted 7/30/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $147,300 - $243,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in statistical leadership for clinical development, including statistical analysis, regulatory submissions, and consulting on clinical trial design. Proficient in mentoring statisticians and ensuring compliance with industry standards.

Highest-signal resume keywords

Statistical AnalysisClinical Trial DesignRegulatory SubmissionsSAS ProgrammingStatistical Methodology

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical LeadershipSample Size CalculationStatistical Analysis Plan AuthoringStatistical Output ReviewRandomization Schedule GenerationBayesian Adaptive Study DesignSurvival AnalysisRepeated Measures AnalysisClinical Study Protocol DevelopmentStatistical Reporting

Soft Skills

Client ConsultingMentoringCollaborationProactive CommunicationTraining

Tools & Technologies

SAS

Industry Keywords

ICH GuidelinesCDISC Data Structures21 CFR Part 11FDA Guidelines

About the role

Key responsibilities & impact

Provides statistical leadership and support for all phases of clinical development
Consulting with clients regarding clinical trial study design and regulatory strategy
Developing and reviewing statistical methods of clinical study protocols
Providing and/or verifying sample size calculations
Authoring statistical analysis plans of complex study design
Reviewing statistical analysis plans written by other biostatisticians
Reviewing statistical output to ensure accuracy
Reviewing statistical sections of clinical study reports
Generating and/or verifying randomization schedules
Providing statistical analysis and reporting to Data Monitoring Committees (DMCs) as the unblinded reporting biostatistician
Working proactively with sponsors, internal study team, and external vendors
Serving as a Subject Matter Expert (SME) and developing/reviewing procedural documents and working on new initiatives
Mentoring and training other statisticians
Attending bid defense meetings for complex programs
Other duties as assigned

Requirements

What you’ll need

Senior Principal Biostatistician level: Master's degree or equivalent in Statistics, Biostatistics, or related field with 12+ years of experience; PhD degree in Statistics, Biostatistics, or related field with 9+ years of experience
Principal Biostatistician level: Master's degree or equivalent in Statistics, Biostatistics, or related field with 10+ years experience; PhD degree in Statistics, Biostatistics, or related field with 7+ years experience
Broad experience with regulatory submissions
Extensive experience consulting with clients regarding clinical trial study design and regulatory strategy
Superior understanding of a statistical methodology (e.g., Bayesian adaptive study design, Survival analysis, Repeated measures)
Sound knowledge of industry standards such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines
Experience with SAS

Benefits

Comp & perks

This role is also eligible for a discretionary annual bonus
Health insurance
Retirement savings benefits
Life insurance
Disability benefits
Parental leave
Paid time off for sick leave and vacation