Oncology Clinical Researcher

Oncology Clinical Researcher (AI Training) About The Role What if your deep expertise in cancer clinical trials could directly shape how AI reasons about oncology — influencing the tools that will define the next era of cancer research and care? We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into AI-driven research workflows. You'll evaluate, validate, and improve how advanced AI systems understand oncology trial data — ensuring that the science behind cutting-edge AI reflects genuine regulatory, clinical, and scientific standards. This is a fully remote, flexible contract role built for experienced oncology professionals who want to do meaningful work on their own schedule. 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 criteria, and regulatory compliance considerations Analyze cancer trial data covering safety endpoints, efficacy outcomes, and biomarker results to assess treatment performance 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 validity, and regulatory alignment Apply your domain expertise to improve how 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 background in analyzing clinical oncology data — including primary and secondary endpoints, safety profiles, and biomarkers Familiar with regulatory submission standards for agencies such as the FDA or EMA Detail-oriented and rigorous — you hold AI-generated content to the same standards you'd apply in a real clinical setting Comfortable working independently on structured, task-based assignments Nice to Have Prior experience with data annotation, data quality evaluation, or AI model assessment workflows Background in oncology publications, clinical decision support, or medical writing Experience across multiple cancer types or therapeutic modalities Why Join Us Work directly on frontier AI systems that are transforming how cancer research is understood and conducted Influence how AI models reason about real oncology data — at a scale no individual trial could achieve Fully remote and flexible — work when and where it suits you Freelance autonomy with the structure of meaningful, impactful work Collaborate with world-leading AI research teams and labs Potential for ongoing work and contract extension as new projects launch

You will design and evaluate oncology clinical trial frameworks and analyze cancer trial data to assess treatment performance. Additionally, you will review AI-generated oncology insights for clinical accuracy and improve AI models' understanding of real-world oncology data.

Candidates should have experience in designing and managing oncology clinical trials and a strong background in analyzing clinical oncology data. Familiarity with regulatory submission standards and detail-oriented rigor are also essential.

• Fully remote work • Flexible schedule • Freelance autonomy • Potential for ongoing work

Identified from the job description. Confirm important requirements above.

• Oncology Clinical Trials
• Data Analysis
• Regulatory Compliance
• Clinical Research
• AI Model Assessment
• Patient Enrollment
• Safety Endpoints
• Efficacy Outcomes
• Biomarker Results
• Medical Writing
• Data Quality Evaluation
• Clinical Decision Support
• Cancer Types
• Therapeutic Modalities

Minimum experience

5+ years