ContractRemoteExpired

Biostatistician

micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI benchmarking. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.

This job opportunity has expired.

The listing's valid-through date has passed. Its details remain available as a historical reference.

View Current Jobs

Salary

$60 - $100 / hour

Department

Biostatistics & Clinical Research

Experience

4+ years

Responsibilities

Design and author expert-level evaluation tasks simulating real-world biostatistics challenges, including clinical trial analysis, regulatory submission reviews, and observational study assessments.
Source, construct, and curate authentic datasets including trial data, patient records, and protocol documents for evaluation tasks.
Define correct methodological solutions and defensible clinical interpretations for each evaluation scenario.
Develop comprehensive grading rubrics with 35 or more criteria to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.
Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.
Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.

Skills

BiostatisticsMethodological RigorClinical InterpretationRegulatory SensitivityClinical Trial AnalysisClinical Study DesignObservational ResearchRegulatory DocumentationRPythonSASStata

Requirements

MS or PhD in biostatistics, statistics, epidemiology, or a related quantitative field.
4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts.
Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.
Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets.
Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.
Experience preparing submission-ready deliverables for regulatory agencies such as FDA or EMA is a plus.
Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.

Benefits

Remote contractor opportunity
Contribute biostatistics expertise to next-generation AI training
Help develop advanced AI benchmarking tasks based on real-world clinical research
Work with realistic clinical trial, observational research, and regulatory scenarios
Output-based compensation for tasks meeting project specifications
Opportunity to influence AI evaluation through rigorous biostatistical and clinical expertise

Biostatistician

Responsibilities

Design and author expert-level evaluation tasks simulating real-world biostatistics challenges, including clinical trial analysis, regulatory submission reviews, and observational study assessments.

Source, construct, and curate authentic datasets including trial data, patient records, and protocol documents for evaluation tasks.

Define correct methodological solutions and defensible clinical interpretations for each evaluation scenario.

Develop comprehensive grading rubrics with 35 or more criteria to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.

Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.

Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.

Requirements

MS or PhD in biostatistics, statistics, epidemiology, or a related quantitative field.

4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts.

Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.

Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets.

Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.

Experience preparing submission-ready deliverables for regulatory agencies such as FDA or EMA is a plus.

Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.

Benefits

Remote contractor opportunity

Contribute biostatistics expertise to next-generation AI training

Help develop advanced AI benchmarking tasks based on real-world clinical research

Work with realistic clinical trial, observational research, and regulatory scenarios

Output-based compensation for tasks meeting project specifications

Opportunity to influence AI evaluation through rigorous biostatistical and clinical expertise