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Grading Contractor In Jobs in Chicago, IL (NOW HIRING)

YO AI Labs

Hematology Expert - Remote

Chicago, IL · Remote

$150 - $200/hr

Contractor Location: Remote Job Overview We are seeking experienced Clinicians specializing in ... Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution ...

Stanley Consultants

Water Resources Engineer

Chicago, IL · On-site

$94.10 - $120.88/hr

Familiarity with site grading design, surface runoff management, detention design, conveyance ... The contractor will not discharge or in any other manner discriminate against employees or ...

YO AI Labs

Federal Reporting Expert - Remote

Chicago, IL · Remote

$40 - $60/hr

Contractor Location: Remote - United States Job Overview We are seeking experienced Federal ... Evaluate sample reports using grading criteria and quality standards. * Develop reference responses ...

Stantec

Railway Engineer

Chicago, IL · On-site

$70 - $90/hr

... utilities, plans/profiles, grading, cross sections, diagrams, and details as required ... Participate in meetings with clients, contractors, agency personnel, and governing entities.

micro1 AI

Legal AI Trainer - Remote

Elgin, IL · Remote

$90 - $150/hr

Contractor Location: Remote We are seeking seasoned Funds Attorneys for a part-time role at the ... In this role, you will review, assess, and contribute to contract redlining workflows used to train ...

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Infographic showing various Grading Contractor In job openings in Chicago, IL as of August 2026, with employment types broken down into 70% Full Time, 9% Part Time, and 21% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution.

Hematology Expert - Remote

YO AI Labs

Chicago, IL • Remote

$150 - $200/hr

Full-time

Posted 24 days ago

Job description

Job Title: Hematology Expert Remote

Job Type: Contractor
Location: Remote

Job Overview

We are seeking experienced Clinicians specializing in Oncology and Hematology to contribute their medical expertise to an innovative healthcare AI project. In this role, you will help improve next-generation AI systems by evaluating clinical content, reviewing trial data, and providing expert medical judgment. No prior AI experience is required—your clinical expertise and domain knowledge are what matter most.

Key Responsibilities

  • Author and review clinical evaluation tasks requiring advanced oncology and hematology expertise.

  • Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess medical accuracy.

  • Evaluate the clinical relevance of efficacy and safety conclusions, including endpoints and treatment outcomes.

  • Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution, and patient safety narratives.

  • Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible interpretations.

  • Provide structured, guideline-based written explanations of clinical reasoning and findings.

  • Support AI model training by delivering high-quality clinical evaluations and expert feedback.

Required 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 & Attribution

Preferred Qualifications

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

  • 5+ years of post-training clinical experience.

  • Direct experience with clinical trials as an investigator, sub-investigator, medical monitor, safety physician, or clinical development physician.

  • Experience reviewing clinical trial documents, including protocols, investigator brochures, clinical study reports, safety narratives, and DSMB/IDMC materials.

  • Strong understanding of oncology and hematology response criteria and clinical endpoints.

  • Excellent written communication skills with the ability to explain complex clinical concepts clearly.

  • Experience in medical monitoring, medical director roles, adjudication committees, or independent review committees is preferred.

  • Peer-reviewed publications or authorship of clinical trial manuscripts is a plus.

  • Experience with AI-assisted clinical review tools is an advantage.