Oncology / Hematology Clinician for AI Training

Role Overview

Apply oncology and hematology expertise to help develop and evaluate healthcare AI through clinically rigorous, real-world assessments. This remote contract role focuses on translating nuanced clinical judgment into clear written evaluations. Prior AI experience is not required.

Key Responsibilities

• Author and review evaluation tasks using Clinical Study Reports, periodic safety reports, and regulatory correspondence in oncology and hematology.
• Assess whether efficacy and safety conclusions are clinically defensible, including the clinical significance of endpoints and effect sizes.
• 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 in light of new events, and the realism of 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 to non-clinical audiences.

Qualifications

• Specialist registration or board certification in medical oncology and/or hematology, with at least 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 in CTCAE grading; RECIST, Lugano, IMWG, IWCLL, and ELN response criteria; and outcome endpoints including ORR, DoR, PFS, OS, and MRD.
• Hands-on experience reviewing protocols, investigator brochures, Clinical Study Reports, safety narratives, and DSMB or IDMC materials.
• Excellent structured written communication and the ability to explain complex clinical reasoning clearly for non-clinical readers.
• Experience in medical monitoring or medical-director roles for oncology or hematology programs is preferred, as is participation in IDMC, DSMB, adjudication, or independent review committees.
• Peer-reviewed publications or authorship on clinical-trial manuscripts is preferred.

Work Terms

• Remote contract engagement.

Compensation

• $160 to $200 per hour.

Eligibility

• Applicants should have direct clinical-trial involvement in one or more relevant investigator or sponsor-side clinical roles.