Oncology Clinical Researcher - #189862

Alignerr


Date: 2 hours ago
City: Birmingham
Contract type: Contractor
Remote
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 systems that will transform how we research, diagnose, and treat cancer?

We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll evaluate and validate AI-generated oncology insights, ensuring that the models being built by the world's leading AI labs are grounded in genuine scientific, regulatory, and clinical expertise.

This is a fully remote, flexible contract role. If you've spent years designing trials, interpreting endpoints, and navigating regulatory submissions — this is a rare opportunity to apply that expertise at the frontier of AI.

  • 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 — including protocol development, patient enrollment frameworks, and compliance standards — to assess and improve AI outputs
  • Analyze AI-generated interpretations of cancer trial data, including efficacy endpoints, safety profiles, and biomarker results
  • Evaluate whether AI-produced regulatory and scientific content meets the standards required for FDA/EMA submissions and clinical decision-making
  • Provide structured, expert feedback that directly shapes how frontier AI models understand and reason about oncology
  • 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 — endpoints, safety profiles, and biomarkers
  • Familiar with regulatory submission standards for agencies such as the FDA or EMA
  • Detail-oriented and methodical — you hold clinical outputs to a high standard
  • Comfortable evaluating complex scientific content and articulating clear, reasoned feedback
  • No prior AI experience required — your clinical expertise is what matters

Nice to Have

  • Prior experience with data annotation, data quality, or evaluation workflows
  • Background in translational oncology or biomarker research
  • Experience contributing to regulatory submissions or clinical publications
  • Familiarity with AI tools or content evaluation platforms as an end user

Why Join Us

  • Work directly on frontier AI systems being built to transform cancer research
  • Influence how AI models understand real oncology data — your expertise leaves a lasting mark
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, expert-level work
  • Collaborate with a global network of specialists across medicine and science
  • Potential for ongoing work and contract extension as new projects launch

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