CONTRACTORRemoteActive
Biostatistician
micro1 is engaging Biostatisticians to contribute to a customer project focused on advanced AI benchmarking. Contributors will apply expert biostatistical knowledge to design realistic evaluation tasks covering clinical trial analysis, regulatory submission reviews, and observational study assessments. The work includes curating authentic clinical datasets and documentation, defining defensible methodological solutions and clinical interpretations, developing detailed grading rubrics, and ensuring evaluation tasks reflect the complexity of real-world biostatistics practice and applicable regulatory and scientific standards. No prior AI experience is required.
Salary
USD60 - USD100 / hour
Department
Biostatistics & AI Evaluation
Experience
4+ years of biostatistics experience in pharmaceutical, contract research, hospital, or academic medical environments, with an MS or PhD in biostatistics, statistics, or epidemiology preferred
Curated by Farooq77 Jobs
Role fit snapshot
- Engagement
- Remote contractor | micro1 application platform
- Experience
- Minimum recorded experience: 4+ years of biostatistics experience in pharmaceutical, contract research, hospital, or academic medical environments, with an MS or PhD in biostatistics, statistics, or epidemiology preferred
- Core expertise
- Biostatistics & AI Evaluation | Biostatistics | Statistical Analysis | Methodological Rigor
- Named tools
- Python | R | Stata
- Expected work/output
- Evaluation tasks | Grading rubrics
- Geographic eligibility
- Not specified beyond Remote
- Listing dates
- Posted 2026-09-17 | Valid through 2026-10-17
- 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.
- Create scenarios involving clinical trial analysis, regulatory submission reviews, and observational study assessments.
- Source, construct, and curate authentic datasets for evaluation tasks.
- Work with trial data, patient records, and clinical protocol documents.
- Define correct methodological solutions for each evaluation scenario.
- Develop defensible clinical interpretations of statistical findings.
- Develop comprehensive grading rubrics containing 35 or more criteria.
- Evaluate AI agent performance based on methodological rigor and clinical reasoning.
- Ensure tasks reflect the complexity and depth of real-world biostatistics practice.
- Avoid simplified or textbook-style evaluation examples.
- Collaborate with project stakeholders to align deliverables with regulatory standards.
- Ensure deliverables meet relevant scientific standards.
- Contribute expert biostatistical knowledge to AI benchmarking and training.
- Create detailed technical documentation and evaluation materials.
- Meet minimum weekly task submission requirements.
- Begin assigned tasks within 24–48 hours after completing onboarding if selected.
Skills
BiostatisticsStatistical AnalysisMethodological RigorClinical InterpretationRegulatory SensitivityClinical Study DesignClinical Trial AnalysisObservational ResearchObservational Study AssessmentRegulatory DocumentationRegulatory Submission ReviewClinical ResearchEpidemiologyRPythonSASStataClinical Data AnalysisEpidemiological Data AnalysisPatient RecordsTrial DataProtocol DocumentsMethodological EvaluationClinical ReasoningAI BenchmarkingAI Agent EvaluationGrading Rubric DesignTechnical DocumentationRegulatory StandardsScientific StandardsFDAEMAData CurationResearch MethodologyAttention to DetailWritten Communication
Requirements
- MS or PhD in biostatistics, statistics, epidemiology, or a related field.
- 4+ years of professional experience in pharmaceutical, contract research, hospital, or academic medical contexts.
- Demonstrated command of clinical study design.
- Experience with regulatory documentation and submission processes.
- Strong knowledge of observational research methodologies.
- Advanced proficiency in R, Python, SAS, or Stata.
- Experience applying statistical programming to real clinical or epidemiological datasets.
- Strong methodological rigor and attention to statistical detail.
- Strong clinical interpretation skills.
- Strong understanding of regulatory sensitivity in clinical research.
- Experience preparing submission-ready deliverables for regulatory agencies such as FDA or EMA is a plus.
- Excellent written communication skills.
- Ability to author detailed grading rubrics.
- Ability to produce technical documentation.
- Ability to work independently in a remote environment.
- Ability to meet minimum weekly task submissions.
- No prior AI experience is required.
Benefits
- Fully remote contractor opportunity.
- Listed compensation range of $60–$100 per hour equivalent.
- Output-based compensation paid per task meeting project specifications.
- Opportunity to contribute biostatistical expertise to advanced AI benchmarking.
- Opportunity to design realistic clinical and biostatistical evaluation tasks.
- Opportunity to work with clinical trial data, patient records, and protocol documentation.
- Opportunity to develop detailed AI evaluation rubrics focused on methodological rigor and clinical reasoning.
- Work aligned with real-world regulatory and scientific standards.
- Remote collaboration with project stakeholders.
- Roles are typically filled within 48 hours.
- Expected task start within 24–48 hours after onboarding if selected.
- No prior AI experience required.
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.