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, adaptable contract role built for oncology professionals who want to do meaningful work on their own terms.
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
📌 Oncology Clinical Researcher (España)
🏢 Alignerr
📍 España
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