Biostatistician

SaidGig

New York (NY)

Remote

USD 83,000 - 138,000

Part time

5 days ago
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Job summary

SaidGig is seeking a remote biostatistics contractor to design and author advanced evaluation tasks based on clinical analyses and regulatory considerations. You will source authentic task materials and craft defensible interpretations, with rubrics for rigor.

Collaboration with stakeholders ensures alignment with scientific and regulatory standards. Ideal candidates hold an MS/PhD in biostatistics or epidemiology, 4+ years in pharma/CRO settings, and strong writing skills to produce

Qualifications

  • MS or PhD in biostatistics, statistics, or epidemiology.
  • At least 4 years of experience in pharmaceutical, contract research, hospital, or academic medical settings.
  • Demonstrated expertise in clinical study design, regulatory documentation, and observational research methods.
  • Advanced proficiency using R, Python, SAS, or Stata with real clinical or epidemiological datasets.
  • Strong methodological rigor, clinical interpretation skills, regulatory sensitivity, and biostatistics expertise.
  • Excellent written communication skills and the ability to produce detailed technical documentation and grading rubrics.
  • Experience creating submission-ready materials for regulatory agencies such as the FDA or EMA is preferred.

Responsibilities

  • Design and author expert-level evaluation tasks based on clinical trial analyses, regulatory submission reviews, and observational study assessments.
  • Source, construct, and curate authentic task materials, including trial data, patient records, and protocol documents.
  • Define methodologically sound solutions and defensible clinical interpretations for each scenario.
  • Create comprehensive rubrics with 35 or more items to assess methodological rigor and clinical reasoning.
  • Ensure tasks reflect the complexity of real-world biostatistics practice rather than simplified textbook examples.
  • Collaborate with project stakeholders to align deliverables with scientific and regulatory standards.

Skills

Biostatistics
Regulatory awareness
Clinical interpretation
Technical writing

Education

MS or PhD in biostatistics, statistics, or epidemiology

Tools

R
Python
SAS
Stata

Job description

Apply biostatistics expertise to develop rigorous evaluations that help train and assess next-generation AI systems. This remote contract role focuses on realistic clinical and epidemiological scenarios, with no prior AI experience required.

Key Responsibilities
  • Design and author expert-level evaluation tasks based on clinical trial analyses, regulatory submission reviews, and observational study assessments.
  • Source, construct, and curate authentic task materials, including trial data, patient records, and protocol documents.
  • Define methodologically sound solutions and defensible clinical interpretations for each scenario.
  • Create comprehensive rubrics with 35 or more items to assess methodological rigor and clinical reasoning.
  • Ensure tasks reflect the complexity of real-world biostatistics practice rather than simplified textbook examples.
  • Collaborate with project stakeholders to align deliverables with scientific and regulatory standards.
Qualifications
  • MS or PhD in biostatistics, statistics, or epidemiology.
  • At least 4 years of experience in pharmaceutical, contract research, hospital, or academic medical settings.
  • Demonstrated expertise in clinical study design, regulatory documentation, and observational research methods.
  • Advanced proficiency using R, Python, SAS, or Stata with real clinical or epidemiological datasets.
  • Strong methodological rigor, clinical interpretation skills, regulatory sensitivity, and biostatistics expertise.
  • Excellent written communication skills and the ability to produce detailed technical documentation and grading rubrics.
  • Experience creating submission-ready materials for regulatory agencies such as the FDA or EMA is preferred.
Work Terms
  • Remote, independent contractor engagement.
  • Work is output-based, and the time needed may vary by experience and workflow.
  • Minimum submission requirements apply, including a minimum number of tasks per week.
  • Selected candidates should be ready to begin initial tasks within 24 to 48 hours after onboarding.
Compensation
  • $60 to $100 per hour.
  • Payment is made per task that meets project specifications.
Eligibility

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