Oncology Clinical Researcher
- Design and run oncology clinical trials by developing study protocols, overseeing patient enrollment, and ensuring compliance with regulatory and ethical standards.
- Analyze cancer trial data, including safety, efficacy, and biomarker results, to evaluate how well treatments perform.
- Translate trial outcomes into regulatory and scientific reports used for FDA/EMA submissions, publications, and clinical decision-making.
- Review and evaluate AI-generated clinical insights for accuracy, clinical relevance, and regulatory alignment.
- Experience 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.
- Familiarity with regulatory submission standards for agencies such as the FDA or EMA.
- Prior experience with data annotation, data quality, or evaluation systems
- Competitive pay and flexible remote work.
- Work directly on frontier AI systems transforming cancer research.
- Influence how AI models understand and reason about real oncology data.
- Freelance perks: autonomy, flexibility, and global collaboration.
- Potential for contract extension.
- Submit your resume
- Complete a short screening
- Project matching and onboarding
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