- 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 robust 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