Oncology/Hematology Clinician for AI Training

Role Overview

Apply oncology and hematology expertise to develop and review clinically rigorous evaluation work that helps train advanced healthcare AI systems. This remote contract role centers on interpreting clinical-trial evidence, safety data, and regulatory materials. Prior AI experience is not required.

Key Responsibilities

• Author and review evaluation tasks requiring nuanced clinical judgment, 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 benefit.
• Evaluate dose escalation, dose-limiting toxicities, dose modifications, adverse-event grading and attribution, and the consistency of patient narratives.
• Analyze benefit-risk reasoning, including the durability of conclusions as new events emerge and the realism of proposed management strategies.
• Identify clinically implausible or internally inconsistent content while distinguishing it from legitimate clinical variation.
• Provide structured, guideline-based written rationales that explain clinical interpretations and limitations clearly for non-clinical audiences.

Qualifications

• Specialist registration or board certification in medical oncology and/or hematology, with 5+ years of post-training clinical experience.
• Clinical-trial experience as an investigator, sub-investigator, sponsor-side medical monitor, safety physician, or clinical development physician.
• Proficiency with CTCAE grading; RECIST, Lugano, IMWG, IWCLL, and ELN response criteria; and ORR, DoR, PFS, OS, and MRD endpoints.
• Hands-on experience reviewing protocols, investigator brochures, Clinical Study Reports, safety narratives, and/or DSMB or IDMC materials.
• Strong clinical reasoning, attention to detail, critical thinking, and problem-solving skills.
• Excellent structured written communication, including the ability to explain complex clinical reasoning to non-clinical readers.
• Experience in medical monitoring or as a medical director for oncology or hematology programs, plus participation in IDMC, DSMB, adjudication, or independent review committees.
• A peer-reviewed publication record or authorship on clinical-trial manuscripts. Exposure to AI-assisted clinical work is also valued.

Work Terms

• Remote contract engagement.

Compensation

• $160 to $200 per hour.