Oncology Clinical Researcher

- Organization: Alignerr - Type: Hourly Contract - Location: Remote - Commitment: 10–40 hours/week

What You'll Do

* Review and evaluate AI-generated oncology content for clinical accuracy, scientific validity, and regulatory alignment * Apply your trial design expertise to assess study protocols, patient enrollment logic, and compliance with ethical and regulatory standards * Analyze AI outputs related to cancer trial data — including safety profiles, efficacy endpoints, and biomarker findings * Evaluate AI-generated regulatory and scientific reporting against FDA/EMA submission standards * Provide structured, expert feedback that directly improves how frontier AI systems reason about oncology * 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 oncology clinical data — including endpoints, safety profiles, and biomarkers * Familiar with regulatory submission standards for agencies such as the FDA or EMA * Detail-oriented, methodical, and capable of delivering clear, well-reasoned evaluations * Able to translate complex clinical and scientific knowledge into structured, actionable feedback

Nice to Have

* Prior experience with data annotation, data quality, or AI evaluation workflows * Background in translational oncology or clinical pharmacology * Experience contributing to publications, regulatory dossiers, or scientific communications

Why Join Us

* Work directly on frontier AI systems transforming how the world understands cancer research * Fully remote and flexible — work when and where it suits you * Freelance autonomy with the structure of meaningful, expert-level work * Influence how AI models reason about real oncology data at the cutting edge of science * Collaborate with world-leading AI research teams and labs * Potential for ongoing work and contract extension as new projects launch