Oncology / Hematology Clinician for AI Training

Apply oncology and hematology expertise to help evaluate and improve healthcare-focused AI systems through clinically rigorous, real-world input. This remote contract role centers on assessing complex clinical-trial evidence and translating expert judgment into clear written feedback. Prior AI experience is not required. Key Responsibilities

• Author and review evaluation tasks requiring nuanced clinical judgment in oncology and hematology, using clinical study reports, periodic safety reports, and regulatory correspondence.
• Assess whether efficacy and safety conclusions are clinically defensible, including whether endpoints and effect sizes demonstrate meaningful clinical significance.
• Evaluate dose escalation, dose-limiting toxicities, dose modifications, adverse-event grading and attribution, and the consistency of patient narratives.
• Review benefit-risk reasoning, the durability of conclusions as new events emerge, and the realism of proposed clinical management strategies.
• Identify clinically implausible or internally inconsistent content while distinguishing it from legitimate clinical variation.
• Provide structured, guideline-based rationales that explain the strengths and limitations of clinical interpretations for non-clinical audiences.

• Specialist registration or board certification in medical oncology, hematology, or both, with at least 5 years of post-training clinical experience.
• Direct clinical-trial experience as an investigator, sub-investigator, sponsor-side medical monitor, safety physician, or clinical development physician.
• Proficiency in CTCAE grading; RECIST, Lugano, IMWG, IWCLL, and ELN response criteria; and outcome-endpoint analysis including ORR, DoR, PFS, OS, and MRD.
• Hands-on experience reviewing protocols, investigator brochures, clinical study reports, safety narratives, or DSMB/IDMC materials.
• Strong clinical reasoning, attention to detail, critical thinking, problem identification and resolution, and structured written communication.
• Ability to explain complex clinical information clearly to non-clinical readers.
• Preferred experience in medical monitoring or as a medical director for oncology or hematology programs, including participation in IDMC, DSMB, adjudication, or independent review committees.
• Peer-reviewed publication record or authorship on clinical-trial manuscripts; exposure to AI-assisted clinical review is beneficial.

• Remote independent-contractor engagement.

• $160 to $200 per hour.