Oncology Clinical Researcher
About this role
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? We're looking for experienced Oncology Clinical Researchers to bring rigorous, real-world clinical trial knowledge into cutting-edge AI development workflows. You'll 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 You'll 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 you'd 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 world's 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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