Contract
Posted Nov 3, 2026
Job Description
Job Type: Contractor
We are looking for experienced clinicians specializing in Oncology and Hematology to lend their medical expertise to a groundbreaking healthcare AI project. In this role, you will play a pivotal part in enhancing next-generation AI systems by evaluating clinical content, analyzing trial data, and offering your expert medical judgment. Previous AI experience is not required—your clinical expertise and domain knowledge are the most valuable assets you bring to this position.
Key Responsibilities:
• Author and review clinical evaluation tasks that require advanced oncology and hematology expertise.
• Analyze clinical study reports, safety reports, regulatory documents, and trial materials to ensure medical accuracy.
• Evaluate the clinical relevance of efficacy and safety conclusions, including endpoints and treatment outcomes.
• Assess dose escalation strategies, dose-limiting toxicities, and adverse event grading along with patient safety narratives.
• Review benefit-risk assessments and pinpoint clinically inconsistent or implausible interpretations.
• Provide structured, guideline-based written explanations of your clinical reasoning and findings.
• Support AI model training by delivering high-quality clinical evaluations and expert feedback.
Required Skills:
• Clinical expertise in Oncology
• Clinical expertise in Hematology
• Clinical Trial Evaluation knowledge
• CTCAE Grading familiarity
• RECIST knowledge
• Lugano Criteria understanding
• IMWG Criteria expertise
• IWCLL Criteria knowledge
• ELN Criteria familiarity
• Outcome Endpoint Analysis including ORR, DoR, PFS, OS, and MRD
• Dose Escalation Assessment skills
• Adverse Event Grading & Attribution proficiency
Preferred Qualifications:
• Board certification or specialist registration in Medical Oncology and/or Hematology.
• 5+ years of post-training clinical experience.
• Direct experience as an investigator or sub-investigator in clinical trials.
• Familiarity with clinical trial documents such as protocols, investigator brochures, and clinical study reports.
• Strong understanding of oncology and hematology response criteria and clinical endpoints.
• Excellent written communication skills to convey complex clinical concepts clearly.
• Experience in medical monitoring, medical director roles, or adjudication committees is a plus.
• Peer-reviewed publications or authorship of clinical trial manuscripts are beneficial.
• Experience with AI-assisted clinical review tools is advantageous.
We are looking for experienced clinicians specializing in Oncology and Hematology to lend their medical expertise to a groundbreaking healthcare AI project. In this role, you will play a pivotal part in enhancing next-generation AI systems by evaluating clinical content, analyzing trial data, and offering your expert medical judgment. Previous AI experience is not required—your clinical expertise and domain knowledge are the most valuable assets you bring to this position.
Key Responsibilities:
• Author and review clinical evaluation tasks that require advanced oncology and hematology expertise.
• Analyze clinical study reports, safety reports, regulatory documents, and trial materials to ensure medical accuracy.
• Evaluate the clinical relevance of efficacy and safety conclusions, including endpoints and treatment outcomes.
• Assess dose escalation strategies, dose-limiting toxicities, and adverse event grading along with patient safety narratives.
• Review benefit-risk assessments and pinpoint clinically inconsistent or implausible interpretations.
• Provide structured, guideline-based written explanations of your clinical reasoning and findings.
• Support AI model training by delivering high-quality clinical evaluations and expert feedback.
Required Skills:
• Clinical expertise in Oncology
• Clinical expertise in Hematology
• Clinical Trial Evaluation knowledge
• CTCAE Grading familiarity
• RECIST knowledge
• Lugano Criteria understanding
• IMWG Criteria expertise
• IWCLL Criteria knowledge
• ELN Criteria familiarity
• Outcome Endpoint Analysis including ORR, DoR, PFS, OS, and MRD
• Dose Escalation Assessment skills
• Adverse Event Grading & Attribution proficiency
Preferred Qualifications:
• Board certification or specialist registration in Medical Oncology and/or Hematology.
• 5+ years of post-training clinical experience.
• Direct experience as an investigator or sub-investigator in clinical trials.
• Familiarity with clinical trial documents such as protocols, investigator brochures, and clinical study reports.
• Strong understanding of oncology and hematology response criteria and clinical endpoints.
• Excellent written communication skills to convey complex clinical concepts clearly.
• Experience in medical monitoring, medical director roles, or adjudication committees is a plus.
• Peer-reviewed publications or authorship of clinical trial manuscripts are beneficial.
• Experience with AI-assisted clinical review tools is advantageous.
Additional Details
- City
- Philadelphia
- State
- Pennsylvania
- Country
- US
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