Remote Oncology Clinical Researcher for AI Training

Alignerr Corp.

Charlotte (AR)

Remote

USD 83,000 - 138,000

Part time

34 hours ago
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Job summary

Alignerr is seeking an Oncology Clinical Researcher to review and shape AI-generated oncology content. You will leverage extensive experience in trial design, patient enrollment, and oversight to ensure clinical accuracy and regulatory compliance.

This fully remote contract role offers flexible hours and the chance to influence how AI systems understand real-world cancer data. Ideal candidates will have deep oncology trial expertise, strong analytical skills, and familiarity with FDA/EMA

Qualifications

  • Experienced in designing and managing oncology clinical trials—from protocol development through data readout.
  • Strong analytical background in oncology data, including endpoints, safety profiles, and biomarkers.
  • Familiar with regulatory submission standards for FDA or EMA.
  • Detail-oriented and rigorous; you catch what others miss.
  • Comfortable working independently without hand-holding.

Responsibilities

  • Review and evaluate AI-generated oncology content for clinical accuracy and regulatory alignment.
  • Apply trial experience to assess how AI captures real-world trial design and population considerations.
  • Analyze AI outputs on safety data, endpoints, and biomarkers, flagging gaps or errors.
  • Evaluate AI content against FDA/EMA submission standards and regulatory expectations.
  • Provide expert feedback that shapes how AI models learn to reason about oncology.
  • Work independently and asynchronously on your own schedule.

Job description

Alignerr is seeking an Oncology Clinical Researcher to review and shape AI-generated oncology content. You will leverage extensive experience in trial design, patient enrollment, and oversight to ensure clinical accuracy and regulatory compliance.

This fully remote contract role offers flexible hours and the chance to influence how AI systems understand real-world cancer data. Ideal candidates will have deep oncology trial expertise, strong analytical skills, and familiarity with FDA/EMA

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