Oncology Clinical Researcher for AI Training (Remote)

Alignerr Corp.

Denver (CO)

Remote

USD 83,000 - 165,000

Part time

35 hours ago
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Job summary

Alignerr Corp. is seeking an Oncology Clinical Researcher to shape AI training and evaluation for oncology trials. This remote hourly-contract role focuses on rigorous trial design, data analysis, and regulatory alignment.

You'll design protocols, analyze safety endpoints and biomarkers, translate outcomes for FDA/EMA standards, review AI-generated content for accuracy, and collaborate asynchronously with global teams. 10–40 hours/week, freelance autonomy.

Qualifications

  • Design and manage oncology trial protocols with study design, enrollment criteria, and regulatory considerations.
  • Analyze trial data focusing on safety, efficacy endpoints, and biomarker results.
  • Translate trial outcomes into regulatory and scientific insights aligned with FDA/EMA standards.

Responsibilities

  • Design and evaluate oncology clinical trial protocols, including study design, patient enrollment criteria, and regulatory compliance standards
  • Analyze cancer trial data — covering safety profiles, efficacy endpoints, and biomarker results — to assess treatment performance and clinical validity
  • Translate trial outcomes into clear regulatory and scientific insights aligned with FDA, EMA, and other agency standards
  • Review and critique AI-generated clinical content for scientific accuracy, clinical relevance, and regulatory alignment
  • Help ensure that AI systems reasoning about oncology data reflect real-world standards and best practices

Skills

Oncology trial design
Data analysis
Regulatory knowledge
Independent work

Tools

AI tools
Clinical data platforms

Job description

Alignerr Corp. is seeking an Oncology Clinical Researcher to shape AI training and evaluation for oncology trials. This remote hourly-contract role focuses on rigorous trial design, data analysis, and regulatory alignment.

You'll design protocols, analyze safety endpoints and biomarkers, translate outcomes for FDA/EMA standards, review AI-generated content for accuracy, and collaborate asynchronously with global teams. 10–40 hours/week, freelance autonomy.

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