Biostatistician

Overview

micro1 is engaging Biostatisticians for a customer’s advanced AI benchmarking project. This contractor role focuses on using domain expertise to help train next-generation AI systems through high-quality, real-world biostatistics input. The position is remote and includes 50 openings.

What You'll Do

• Design expert-level evaluation tasks based on real biostatistics work, including clinical trial analysis, regulatory submission review, and observational study assessment.
• Source, construct, and curate authentic datasets such as trial data, patient records, and protocol documents for use in tasks.
• Define correct methodological solutions and defensible clinical interpretations for each scenario.
• Create detailed evaluation rubrics with 35+ items to measure AI performance in methodological rigor and clinical reasoning.
• Build tasks that reflect the depth and complexity of real-world biostatistics practice rather than simplified textbook examples.
• Work with project stakeholders to keep deliverables aligned with regulatory and scientific standards.

Preferred Qualifications

• MS or PhD in biostatistics, statistics, or epidemiology.
• At least 4 years of experience in pharmaceutical, contract research, hospital, or academic medical settings.
• Strong command of clinical study design, regulatory documentation, and observational research methods.
• Advanced proficiency in R, Python, SAS, or Stata using real clinical or epidemiological datasets.
• Ability to write detailed grading rubrics and technical documentation.
• Experience preparing submission-ready materials for regulatory agencies such as the FDA or EMA is a plus.

Compensation

Compensation is output-based and paid per task that meets project specifications. A minimum weekly submission requirement applies.

Availability

Selected experts are expected to begin first tasks within 24–48 hours of onboarding completion.