Oncology Clinical Researcher

Company: Alignerr Agency

  • Location: Germany
  • Work mode: Remote
  • Employment type: Contract
  • Posted: 7 days ago
  • Offer language: English

Job description

Oncology Clinical Researcher (AI Training)

About The Role

What if your deep knowledge of cancer clinical trials could directly shape how AI understands and reasons about oncology — improving the tools that researchers, clinicians, and scientists rely on?

We're looking for Oncology Clinical Researchers to bring real-world clinical expertise into cutting-edge AI development. You'll evaluate, review, and inform AI-generated oncology content — ensuring it reflects the scientific rigor, regulatory standards, and clinical nuance that this field demands.

This is a fully remote, flexible contract role. No AI background needed — just serious expertise in oncology clinical research and a sharp eye for accuracy.

  • 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 expertise in trial design to assess AI outputs against real-world protocol standards — including patient enrollment, endpoint selection, and compliance requirements
  • Analyze AI-generated interpretations of cancer trial data, including safety profiles, efficacy outcomes, and biomarker findings
  • Evaluate whether AI-produced regulatory and scientific summaries meet the standards expected for FDA/EMA submissions and clinical publications
  • Provide structured, detailed feedback that directly improves how AI systems reason about oncology data
  • 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 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 hold AI outputs to the same standards you'd apply in real clinical practice
  • Comfortable providing clear, structured written feedback across a range of oncology topics
  • No prior AI or tech experience required

Nice to Have

  • Prior experience with data annotation, data quality assessment, or AI evaluation workflows
  • Background in translational oncology, clinical pharmacology, or biomarker science
  • Experience contributing to peer-reviewed publications or regulatory submissions
  • Familiarity with multiple oncology therapeutic areas — solid tumors, hematologic malignancies, immunotherapy, etc.

Why Join Us

  • Work directly on frontier AI systems being built to transform cancer research
  • Influence how AI models understand and reason about real oncology data — at the source
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, impactful 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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