Oncology Clinical Researcher

Alignerr

$40–80/h 11 países Horario flexible 10–40 h/semana

Reviewing AI outputs on cancer trials, safety, efficacy and biomarkers against regulatory submission standards. Suits oncology trial professionals who notice when clinical reasoning does not hold up.

Sobre la vacante

Oncology Clinical Researcher (AI Training)
About the Role
What if your deep knowledge of cancer clinical trials could directly shape how AI reasons about oncology — influencing the tools that researchers, clinicians, and scientists rely on worldwide?
We're looking for Oncology Clinical Researchers to bring real-world expertise into AI-driven research workflows. You'll evaluate, guide, and improve how advanced AI systems understand cancer trial data, regulatory science, and clinical evidence — ensuring the AI that's transforming oncology is grounded in rigorous, real-world standards.
This is a fully remote, flexible contract role. No AI background needed — just deep oncology expertise and a sharp eye for clinical and scientific quality.

  • Organization : Alignerr
  • Type : Hourly Contract
  • Location : Remote

- Commitment : 10–40 hours/week

  • Commitment : 10–40 hours/week
  • Review and evaluate AI-generated oncology content for clinical accuracy, scientific rigor, and regulatory alignment
  • Apply your experience designing and managing cancer clinical trials — including protocol development, patient enrollment, and compliance — to assess how well AI handles these workflows
  • Analyze AI outputs covering safety, efficacy, and biomarker data to determine whether they reflect real-world oncology standards
  • Assess the quality of AI-generated regulatory and scientific reports against FDA/EMA submission standards
  • Provide structured, detailed feedback that helps frontier AI systems reason more accurately about cancer research

- Work independently and asynchronously — fully on your own schedule

  • Work independently and asynchronously — fully on your own schedule
  • Experienced in designing and managing oncology clinical trials from protocol development through data readout
  • Strong background in analyzing oncology clinical data, including endpoints, safety profiles, and biomarkers
  • Familiar with regulatory submission standards for agencies such as the FDA or EMA
  • Detail-oriented and rigorous — you notice when clinical or scientific reasoning doesn't hold up
  • Clear and concise written communicator

- No prior AI or tech experience required

  • No prior AI or tech experience required
  • Prior experience with data annotation, data quality, or evaluation systems
  • Background in translational oncology, medical writing, or regulatory affairs
  • Experience working across multiple cancer types or therapeutic areas

- Familiarity with AI tools or clinical decision-support platforms as an end user

  • Familiarity with AI tools or clinical decision-support platforms as an end user
  • Work directly on frontier AI systems that are transforming how the world understands and fights cancer
  • Influence how AI models reason about real oncology data — at a scale no individual trial could reach
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, task-based 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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