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Remote Principal Biostatistician Jobs in Illinois

This is a fully remote, flexible contract role built for experienced clinical researchers who want ... Strong grounding in clinical research methodology, biostatistics, or translational science

Remote Principal Biostatistician information

See Illinois salary details

$54

$81

$113

How much do remote principal biostatistician jobs pay per hour?

As of May 28, 2026, the average hourly pay for remote principal biostatistician in Illinois is $81.94, according to ZipRecruiter salary data. Most workers in this role earn between $70.58 and $94.57 per hour, depending on experience, location, and employer.

What is a Remote Principal Biostatistician job?

A Remote Principal Biostatistician is a senior-level biostatistics professional who analyzes complex medical and clinical trial data while working remotely. They design statistical methodologies, develop study protocols, and ensure data integrity for regulatory submissions. This role often requires collaboration with cross-functional teams, such as data managers and medical writers. Strong expertise in statistical programming (e.g., SAS, R) and regulatory guidelines (e.g., FDA, EMA) is essential. Remote work allows flexibility while maintaining responsibility for high-level statistical oversight and decision-making.

What are the key skills and qualifications needed to thrive in the Remote Principal Biostatistician position, and why are they important?

To thrive as a Remote Principal Biostatistician, you need advanced knowledge of biostatistics, clinical trial design, and statistical data analysis, typically supported by a master's or PhD in statistics, biostatistics, or a related field. Expertise in statistical programming languages such as SAS, R, and experience with clinical data management systems and regulatory guidelines (e.g., ICH/GCP) are essential. Strong leadership, effective communication, and project management skills help you coordinate cross-functional teams and mentor junior statisticians. These competencies ensure high-quality statistical deliverables, regulatory compliance, and successful remote collaboration on complex research projects.

What are the typical daily responsibilities of a Remote Principal Biostatistician?

As a Remote Principal Biostatistician, your daily activities often include designing and overseeing statistical analyses for clinical studies, reviewing protocols and statistical analysis plans, and ensuring adherence to regulatory requirements. You may lead project meetings with cross-functional teams such as data managers, clinical researchers, and programmers, providing statistical expertise and resolving complex methodological issues. Additionally, you are responsible for mentoring junior team members, performing quality control on statistical deliverables, and communicating analysis results to both scientific and non-technical stakeholders. This role relies heavily on self-motivation, organized workflows, and clear virtual communication to ensure high-quality outcomes in a remote environment.
What job categories do people searching Remote Principal Biostatistician jobs in Illinois look for? The top searched job categories for Remote Principal Biostatistician jobs in Illinois are:

Principal Clinical Scientist

Alignerr

Chicago, IL • Remote

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

Principal Clinical Scientist (AI Training)
About the Role
What if your career designing rigorous clinical trials and interpreting regulatory-grade data could directly influence how AI understands medicine? We're looking for a Principal Clinical Scientist to bring senior-level clinical expertise into the development of cutting-edge AI systems - helping ensure these models reason about clinical evidence the way a seasoned scientist would.
This is a fully remote, flexible contract role built for experienced clinical researchers who want to work at the intersection of science and frontier AI. No AI background required - just deep clinical expertise and a sharp eye for scientific rigor.
  • Organization
    : Alignerr
  • Type
    : Hourly Contract
  • Location
    : Remote
  • Commitment
    : 10-40 hours/week
  • What You'll Do
    • Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets for AI training and evaluation
    • Interpret and audit clinical trial results to ensure accuracy, consistency, and alignment with regulatory standards
    • Evaluate AI-generated clinical analyses for scientific soundness and compliance with FDA, EMA, or equivalent agency expectations
    • Provide expert feedback that directly shapes how AI models understand, reason about, and evaluate clinical trial data and outcomes
    • Flag gaps in methodology, data quality, or regulatory relevance across AI-generated clinical content
    Who You Are
    • Senior-level clinical researcher with hands-on experience designing trial protocols for regulatory submission
    • Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies
    • Strong grounding in clinical research methodology, biostatistics, or translational science
    • Naturally rigorous - you hold AI-generated outputs to the same standard you'd apply in a real submission
    • Self-directed and comfortable working independently in an asynchronous environment
    Nice to Have
    • Prior experience with data annotation, data quality evaluation, or AI output assessment
    • Background in pharmacology, oncology, rare disease, or another specialized therapeutic area
    • Familiarity with ICH guidelines, GCP standards, or regulatory submission frameworks
    • Experience working across multidisciplinary research teams
    Why Join Us
    • Work directly on frontier AI systems that are reshaping how clinical and biomedical research is conducted
    • Influence how AI understands and evaluates real-world clinical evidence - at a scale no individual trial could achieve
    • Fully remote and flexible - work when and where it suits you
    • Freelance autonomy with the structure of meaningful, high-impact, task-based work
    • Collaborate with world-leading AI research labs on problems that matter
    • Potential for ongoing work and contract extension as new projects launch