Remote Clinician (Oncology / Hematology)

micro1 is the leading AI data lab for training frontier models and evaluating AI agents. Experts contribute their diverse subject matter knowledge across domains such as finance, healthcare, and STEM engineering. micro1 transforms real-world expertise into high-quality training data, evaluations, and feedback loops that improve how AI systems learn, reason, and perform.

About the role

micro1 is engaging Clinicians (Oncology / Hematology) to contribute to a customer’s project at the forefront of AI in healthcare. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.

Responsibilities

• Author and review evaluation tasks that require nuanced clinical judgment, leveraging Clinical Study Reports, periodic safety reports, and regulatory correspondence in oncology and hematology.
• Assess the clinical defensibility of efficacy and safety conclusions, ensuring endpoints and effect sizes reflect true clinical significance.
• Apply advanced judgment to dose escalation, dose-limiting toxicity, modifications, adverse event grading and attribution, and the coherence of patient narratives.
• Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events, and the realism of described management strategies.
• Identify and flag content that is clinically implausible or internally inconsistent, distinguishing these from legitimate clinical variation.
• Provide structured, guideline-based written rationales that clearly explain the validity or limitations of clinical interpretations for a non-clinical audience.

Requirements

• Specialist registration or board certification in medical oncology and/or hematology, with 5+ years of post-training clinical experience.
• Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical monitor, safety physician, or clinical development physician.
• Proficiency with CTCAE grading, relevant response criteria (RECIST, Lugano, IMWG, IWCLL, ELN), and outcome endpoints (ORR, DoR, PFS, OS, MRD).
• Hands-on experience with trial documents such as protocols, investigator brochures, CSRs, safety narratives, or DSMB/IDMC materials.
• Demonstrated excellence in written communication, with clear, structured explanations of clinical reasoning tailored for non-clinical readers.
• Previous roles in medical monitoring or as medical director on oncology or hematology programs, and committee participation (IDMC, DSMB, adjudication, or independent review committees).
• Peer-reviewed publication record or authorship on clinical trial manuscripts (exposure to AI-assisted clinical review tools is a plus).

Skills

• Clinical oncology
• Clinical hematology
• Clinical trial evaluation
• CTCAE grading
• RECIST, Lugano criteria, IMWG criteria, IWCLL criteria, ELN criteria
• Outcome endpoint analysis (ORR, DoR, PFS, OS, MRD)
• Dose escalation assessment
• Adverse event grading and attribution
• Regulatory document review (CSRs, protocols, investigator brochures, safety narratives, DSMB/IDMC materials)
• Benefit-risk analysis
• Clinical reasoning
• Structured written communication
• Guideline-based documentation
• Explaining complex information to non-clinical audiences
• Medical monitoring committee participation (IDMC, DSMB, adjudication, independent review)
• Peer-reviewed publication
• Attention to detail
• Critical thinking
• Problem identification and resolution

Pay

$160 - $200/hour

Location: Remote
Role Type: Contractor
State: Oregon