Oncology Clinical Researcher

Alignerr Corp.

Auckland

Remote

NZD 147,000 - 270,000

Part time

44 hours ago
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Benefits offered by this job

Fully remote
Freelance autonomy
Potential for ongoing work

Job summary

Alignerr Corp. is seeking an Oncology Clinical Researcher to ensure AI systems understand and reason about cancer care with real-world clinical rigor.

You will review AI-generated oncology content for clinical accuracy, validity, and regulatory alignment, applying trial-design knowledge to assess how well AI captures standard practices. The role is fully remote as an hourly contract, offering 10–40 hours per week and the freedom to work on your own schedule while contributing to frontier AI

Qualifications

  • Experienced in designing and managing oncology trials from protocol development to data readout.
  • Strong understanding of trial endpoints, safety, and biomarkers.
  • Familiar with regulatory submission standards (FDA/EMA).

Responsibilities

  • Review AI-generated oncology content for clinical accuracy and regulatory alignment.
  • Assess trial design aspects: protocol development, enrollment, and endpoint selection.
  • Interpret cancer trial data outputs, including safety, efficacy, and biomarkers, to identify AI gaps.
  • Evaluate AI outputs against FDA/EMA/ICH standards and generate actionable feedback.
  • Provide expert feedback to improve AI models’ oncology reasoning and decision-making.
  • Work independently in a remote, asynchronous setting.

Skills

Oncology trials
Protocol development
Data readout
Regulatory knowledge
Biomarkers

Job description

Oncology Clinical Researcher (AI Training)

What if your deep expertise in cancer clinical trials could directly shape how AI understands and reasons about one of medicine's most complex fields? We're looking for Oncology Clinical Researchers to bring real-world scientific rigor into cutting-edge AI development - ensuring that the models influencing the future of cancer care are grounded in accurate, clinically sound knowledge.

This is a fully remote, flexible contract role built for experienced oncology professionals who want to contribute to frontier AI research without leaving their domain behind.

  • Organization: Alignerr
  • Type: Hourly Contract
  • Location: Remote
  • Commitment: 10-40 hours/week
What You'll Do
  • Review and evaluate AI-generated oncology content for clinical accuracy, scientific validity, and regulatory alignment
  • Apply your knowledge of trial design - including protocol development, patient enrollment, and endpoint selection - to assess how well AI captures real-world oncology research standards
  • Analyze and interpret cancer trial data outputs, including safety profiles, efficacy results, and biomarker findings, to identify errors or gaps in AI reasoning
  • Evaluate AI-generated regulatory and scientific reports against FDA, EMA, and ICH standards
  • Provide structured, expert feedback that directly improves how AI models understand oncology data and clinical decision-making
  • Work independently and asynchronously - fully on your own schedule
Who You Are
  • Experienced in designing and managing oncology clinical trials from protocol development through data readout
  • Strong analytical background in oncology clinical data, including endpoints, safety, and biomarkers
  • Familiar with regulatory submission standards for agencies such as the FDA or EMA
  • Detail-oriented with a methodical approach to evaluating complex scientific content
  • Comfortable working independently in a remote, task-based environment
Nice to Have
  • Prior experience with data annotation, data quality review, or AI evaluation workflows
  • Background in translational oncology or clinical-regulatory writing
  • Experience with biomarker-driven trial design or precision oncology
  • Familiarity with AI tools or content evaluation platforms
Why Join Us
  • Work directly on frontier AI systems that are transforming how cancer research is conducted
  • Influence how the next generation of AI models understands real oncology data, clinical standards, and regulatory science
  • Fully remote and flexible - work when and where it suits you
  • Freelance autonomy with the structure of meaningful, expert-level work
  • Collaborate with world-leading AI research teams and labs
  • Potential for ongoing work and contract extension as new projects launch
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