Medical Oncologist | Remote

Position: Clinician (Oncology / Hematology) Type: Contract Compensation: $160 - $200/hour Location: Remote Commitment: 10-40 hrs/week Role Responsibilities Author and review evaluation tasks requiring nuanced clinical judgment in oncology and hematology. Assess clinical defensibility of efficacy and safety conclusions, ensuring true clinical significance. Apply advanced judgment to dose escalation, toxicity, and adverse event grading. Evaluate benefit-risk reasoning and scrutinize management strategies. Identify and flag clinically implausible content, distinguishing from legitimate variation. Provide structured, guideline-based written rationales for non-clinical audiences. Requirements Specialist registration or board certification in medical oncology and/or hematology with strong relevant experience. Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical monitor. Proficiency with CTCAE grading, relevant response criteria, and outcome endpoints. Hands-on experience with trial documents such as protocols and safety narratives. Demonstrated excellence in written communication tailored for non-clinical readers. Previous roles in medical monitoring or as medical director on oncology or hematology programs. Application Process Easy Apply on LinkedIn Check email for next steps Participate in resume evaluation & interview stage

The role involves authoring and reviewing evaluation tasks to assess the clinical defensibility of efficacy and safety conclusions in oncology and hematology. The clinician will provide structured, guideline-based rationales and identify clinically implausible content.

Candidates must be board-certified in medical oncology or hematology with direct experience as a clinical trial investigator or medical monitor. Proficiency in CTCAE grading and experience with trial protocols and safety narratives is required.

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Medical Oncology
• Hematology
• Clinical Trial Monitoring
• CTCAE Grading
• Benefit-Risk Analysis
• Clinical Judgment
• Medical Writing
• Safety Narratives
• Protocol Review
• Dose Escalation Management

• Healthcare
• Science & Research

Formation minimale

Diplôme professionnel

Expérience minimale

5+ ans

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Niveau d’expérience

Associate

Mode de candidature

La candidature directe est offerte