Oncology Clinical Researcher

About This Role

This role will provide oncology clinical research expertise to AI-driven research. You will lead the design and execution of oncology clinical trials and analyze the resulting data, ensuring regulatory and clinical standards are met.

Responsibilities

• 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

Requirements

• 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

Nice to Have

• Prior experience with data annotation, data quality, or evaluation systems

Benefits