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 affects millions of patients worldwide? We're looking for Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll work alongside leading AI research teams to ensure that the oncology knowledge embedded in frontier AI systems reflects genuine regulatory, scientific, and clinical standards. This is a fully remote, flexible contract role built for experienced oncology professionals who want to extend their impact beyond the clinic. - Organization: Alignerr - Type: Hourly Contract - Location: Remote - Commitment: 10–40 hours/week What You'll Do - Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance considerations - Analyze cancer trial data across safety, efficacy, and biomarker endpoints to assess treatment performance and scientific validity - Translate complex trial outcomes into clear regulatory and scientific narratives aligned with FDA/EMA submission standards - Review and critique AI-generated oncology insights for clinical accuracy, scientific relevance, and regulatory alignment - Help establish the standard for how AI models reason about real-world oncology data 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 biomarker interpretation - Solid familiarity with regulatory submission standards for agencies such as the FDA or EMA - Detail-oriented and comfortable applying scientific judgment in an independent, asynchronous work environment - Motivated by the opportunity to influence how AI understands cancer research Nice to Have - Prior experience with data annotation, data quality review, or AI evaluation workflows - Background in translational oncology or biomarker-driven trial design - Experience preparing or reviewing regulatory submission documents (IND, NDA, BLA, or equivalent) - Familiarity with AI tools or clinical decision-support systems Why Join Us - Work directly on frontier AI systems that are transforming how cancer research is conducted and understood - Influence how AI models interpret and reason about real oncology data — a genuinely rare opportunity - Fully remote and flexible — work on your own schedule, from anywhere - Freelance autonomy with the structure of meaningful, high-impact project work - Collaborate with world-leading AI research labs and oncology professionals globally - Potential for ongoing work and contract extension as new projects launch
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