Remote Hematology & Oncology Clinician for AI Evaluation

YO AI Labs; Dallas (TX); Remote; USD 120,000 - 200,000; Part time

Job summary

YO AI Labs seeks a Hematology Oncology Expert to contribute remote clinical evaluation for an AI healthcare project. You will review trial data, assess medical accuracy, and provide expert judgments without prior AI experience required beyond clinical domain knowledge.

Preferred candidates hold board certification in Medical Oncology and/or Hematology with 5+ years post-training experience, including involvement in clinical trials and safety reporting.

Qualifications

• Board certification in Medical Oncology or Hematology required.
• Direct experience with clinical trials as investigator or monitor preferred.

Responsibilities

• Author and review clinical evaluation tasks with advanced oncology/hematology expertise.
• Analyze clinical study reports, safety documents, and trial materials for medical accuracy.
• Evaluate efficacy/safety conclusions, endpoints, and treatment outcomes.
• Assess dose escalation, DLTs, AEs, attribution, and patient safety narratives.
• Review benefit-risk assessments for consistency and realism.
• Provide guideline-based written explanations of clinical reasoning.
• Support AI model training with high-quality clinical feedback.

Skills

Clinical Oncology

Clinical Hematology

Clinical Trial Evaluation

CTCAE Grading

RECIST

Lugano Criteria

IMWG Criteria

IWCLL Criteria

ELN Criteria

Outcome Endpoint Analysis

Dose Escalation Assessment

Adverse Event Grading

Education

Board certification or specialist registration in Medical Oncology and/or Hematology

Job description

YO AI Labs seeks a Hematology Oncology Expert to contribute remote clinical evaluation for an AI healthcare project. You will review trial data, assess medical accuracy, and provide expert judgments without prior AI experience required beyond clinical domain knowledge.

Preferred candidates hold board certification in Medical Oncology and/or Hematology with 5+ years post-training experience, including involvement in clinical trials and safety reporting.