YO IT CONSULTING Oncology Expert - Remote

YO IT CONSULTING is hiring a remote Oncology/Hematology Clinician on a contract basis to support an innovative healthcare artificial‑intelligence initiative. The project aims to refine next‑generation AI models by incorporating expert medical judgment, and the role is paid at $160‑$200 per hour. The contractor will create and assess clinical evaluation tasks that require deep oncology and hematology knowledge. Daily work includes dissecting clinical study reports, safety dossiers, regulatory filings and trial documentation to verify medical accuracy. You will judge the relevance of efficacy and safety findings, scrutinise dose‑escalation plans, grade adverse events, and evaluate benefit‑risk narratives. Findings must be recorded in clear, guideline‑based written explanations that feed directly into AI model training. Essential qualifications are a board certification or specialist registration in Medical Oncology and/or Hematology, together with at least five years of post‑training practice. Candidates must have hands‑on experience in clinical trials, whether as investigator, sub‑investigator, medical monitor, safety physician or clinical development physician, and a proven track record of reviewing protocols, investigator brochures, study reports, safety narratives and DSMB/IDMC materials. A solid grasp of oncology/hematology response criteria (CTCAE, RECIST, Lugano, IMWG, IWCLL, ELN) and outcome endpoints (ORR, DoR, PFS, OS, MRD) is required, as is the ability to communicate complex clinical concepts in writing. Preferred experience includes roles in medical monitoring, medical directorship, adjudication or independent review committees, as well as authorship of peer‑reviewed publications or trial manuscripts. Familiarity with AI‑assisted clinical review tools is an added advantage. The position is fully remote, offering flexibility within a contract framework. What the role asks for: - Board certification in Medical Oncology and/or Hematology - Minimum 5 years post‑training clinical experience - Experience as clinical trial investigator or sub‑investigator - Experience as medical monitor, safety physician, or clinical development physician - Reviewed protocols, investigator brochures, study reports, safety narratives, DSMB/IDMC materials - Knowledge of CTCAE, RECIST, Lugano, IMWG, IWCLL, ELN criteria - Proficient in ORR, DoR, PFS, OS, MRD endpoint analysis - Excellent written communication of complex clinical concepts - Experience in medical monitoring or medical director roles - Service on adjudication or independent review committees - Peer‑reviewed publications or authorship of trial manuscripts - Familiarity with AI‑assisted clinical review tools