Oncology Clinical Researcher (AI Training)
About The Role
What if your deep expertise in cancer clinical trials could directly shape how AI understands and reasons about oncology — influencing research that could one day transform how cancer is diagnosed and treated?
Were looking for experienced Oncology Clinical Researchers to bring rigorous, real-world clinical trial knowledge into cutting-edge AI development workflows. Youll review, evaluate, and inform AI-generated oncology content — ensuring it reflects the scientific, regulatory, and clinical standards that matter in practice.
This is a fully remote, flexible contract role built for working oncology researchers and clinical scientists who want to engage with frontier AI on their own terms.
* Organization: Alignerr
* Type: Hourly Contract
* Location: Remote
* Commitment: 10–40 hours/week
What Youll Do
* Evaluate AI-generated oncology content for clinical accuracy, scientific rigor, and regulatory alignment.
* Apply your expertise in study protocol design, patient enrollment standards, and trial oversight to assess AI outputs against real-world best practices.
* Analyze and interpret cancer trial data — including safety profiles, efficacy endpoints, and biomarker results — to identify errors or gaps in AI reasoning.
* Review AI-generated regulatory and scientific content for alignment with FDA, EMA, and international submission standards.
* Provide structured, expert feedback that directly improves how AI models understand and generate oncology knowledge.
* 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 clinical trial data, including primary and secondary endpoints, safety reporting, and biomarker analysis.
* Familiar with regulatory submission standards and documentation requirements for agencies such as the FDA or EMA.
* Detail-oriented and rigorous — you hold AI outputs to the same standards youd apply in a real clinical or regulatory setting.
* Able to communicate complex clinical findings clearly in written feedback.
* Self-motivated and comfortable working independently in a remote, asynchronous environment.
Nice to Have
* Prior experience with data annotation, evaluation systems, or AI quality workflows.
* Background in translational oncology, biostatistics, or clinical pharmacology.
* Experience authoring or reviewing regulatory submissions, clinical study reports, or scientific publications.
* Familiarity with AI tools or clinical decision support systems.
Why Join Us
* Work directly on frontier AI systems being developed alongside the worlds leading AI research labs.
* Fully remote and flexible — work when and where it suits you, on a schedule you control.
* Freelance autonomy with the substance of meaningful, high-impact work.
* Contribute to AI that could reshape how cancer research is conducted and communicated at a global scale.
* Potential for ongoing work and contract extension as new oncology AI projects launch.
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