Oncology Clinical Researcher

regulatory, scientific, and clinical standards. Organization: Alignerr | Position: Oncology Clinical Researcher | Type: Hourly Contract | Compensation: $40–$80 /hour | Location: Remote | Commitment: 10–40 hours/week What You’ll Do 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. What We’re Looking For 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. Preferred Prior experience with data annotation, data quality, or evaluation systems Why Join Us 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. Application Process (Takes 15–20 min) Submit your resume Complete a short screening Project matching and onboarding PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity. #J-18808-Ljbffr