Live opening · Posted 2 days ago

Hematology Expert - Remote

ExecutivePlacements.com · Washington, United States (Remote)
Linkedin Yes
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At a glance

The key details from the original listing.

Posted 2 days ago
CompanyExecutivePlacements.com
LocationWashington, United States (Remote)
Work modeYes
SourceLinkedin
Listed2 days ago

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About the role

Description supplied by the original job listing.

Job Description
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.

Work arrangement
Yes

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