Oncology Clinical Researcher

Alignerr Corp.

Spanien

Remote

EUR 83.000 - 165.000

Teilzeit

vor 43 Stunden
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Benefits dieser Stelle

Fully remote
Flexible schedule
Potential for ongoing projects

Zusammenfassung

Alignerr is seeking an Oncology Clinical Researcher for AI training to ensure oncology trial data underpinning AI models meets clinical and regulatory standards. This fully remote, hourly contract role offers flexible scheduling for oncology professionals seeking meaningful, expert-level work on their own terms.

You will design and evaluate protocols, analyze trial data with safety and biomarker focus, and translate findings into regulatory documents for FDA/EMA submissions.

Qualifikationen

  • Experience designing and managing oncology trials from protocol to data readout.
  • Strong analytical background in oncology endpoints, safety, and biomarkers.
  • Familiarity with FDA/EMA regulatory submission standards.
  • Detail-oriented with rigorous evaluation of scientific content.

Aufgaben

  • Design and evaluate oncology trial protocols.
  • Analyze cancer trial data including safety, efficacy, and biomarkers.
  • Translate trial findings into FDA/EMA-ready reports.
  • Review AI-generated clinical insights for regulatory alignment.
  • Shape how AI models interpret real-world oncology data.
  • Work independently and asynchronously on your schedule.

Kenntnisse

Oncology trial design
Data analysis
Regulatory knowledge
Independent worker

Jobbeschreibung

Oncology Clinical Researcher (AI Training)
About The Role

What if your deep expertise in cancer clinical trials could directly influence how AI understands and reasons about oncology — at a global scale?

We're looking for Oncology Clinical Researchers to bring real-world rigor to AI-driven research workflows. You'll work with leading AI labs to ensure the models being trained on oncology data reflect genuine clinical, regulatory, and scientific standards — the kind of nuance only a seasoned expert can provide.

This is a fully remote, flexible contract role built for oncology professionals who want to do meaningful work on their own terms.

  • Organization: Alignerr
  • Type: Hourly Contract
  • Location: Remote
  • Commitment: 10–40 hours/week
What You'll Do
  • Design and evaluate oncology clinical trial protocols, ensuring alignment with regulatory and ethical standards
  • Analyze cancer trial data — including safety outcomes, efficacy endpoints, and biomarker results — to assess treatment performance
  • Translate trial findings into regulatory and scientific reports consistent with FDA/EMA submission standards
  • Review and evaluate AI-generated clinical insights for accuracy, scientific validity, and regulatory alignment
  • Help shape how frontier AI models understand and reason about real-world 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 analytical background in oncology clinical data, including endpoints, safety profiles, and biomarkers
  • Familiar with regulatory submission standards for agencies such as the FDA or EMA
  • Detail-oriented with a systematic, rigorous approach to evaluating scientific content
  • Comfortable working independently and delivering structured, high-quality outputs
Nice to Have
  • Prior experience with data annotation, data quality review, or AI evaluation systems
  • Background in translational oncology or biomarker-driven trial design
  • Familiarity with AI tools or clinical data platforms
  • Experience writing or reviewing publications for peer-reviewed oncology journals
Why Join Us
  • Work directly on frontier AI systems being developed alongside the world's leading research labs
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the substance of impactful, expert-level work
  • Influence how AI models interpret and apply real oncology evidence
  • Contribute to technology that could meaningfully advance how cancer research is conducted and understood
  • Potential for ongoing work and contract extension as new projects launch
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