ContractRemoteActive
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.
Salary
$60 - $100 / hour
Department
Biostatistics & Clinical Research
Experience
4+ years
Curated by Farooq77 Jobs
Role fit snapshot
- Engagement
- Remote contractor | micro1 application platform
- Experience
- Minimum recorded experience: 4+ years
- Core expertise
- Biostatistics & Clinical Research | Biostatistics | Methodological Rigor | Clinical Interpretation
- Named tools
- Python | R | Stata
- Expected work/output
- Evaluation tasks | Grading rubrics
- Geographic eligibility
- Not specified beyond Remote
- Listing dates
- Posted 2026-08-13 | Valid through 2026-09-13
- Compensation
- Recorded compensation: $60-$100/hourOutput-based compensation is also recorded in the listing.
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
Before you apply
- Confirm that your location is eligible for the role.
- Confirm the employment or contract type.
- Verify the current compensation at the official source.
- Review the required skills and experience.
- Check that the listing is still open before applying.
- Never pay a fee to submit a job application.