Medical Hematology | Remote

Crossing Hurdles; Canada; On-site; CAD 220,000 - 276,000; Part time

Job summary

Crossing Hurdles seeks a Clinician specializing in Oncology and Hematology for a remote contract role. This position emphasizes evaluating clinical trials, applying advanced judgment to dose escalation, toxicity grading, and safety assessments.

Reqs include specialist board certification, direct trial involvement, CTCAE proficiency, and strong written communication for non-clinical audiences. 10-40 hrs/week, $160–$200/hour.

Qualifications

• Specialist registration or board certification in medical oncology and/or hematology.
• Direct involvement in clinical trials as investigator or monitor.
• Proficiency with CTCAE grading, response criteria, and endpoints.
• Hands-on experience with trial documents (protocols, safety narratives).
• Excellent written communication for non-clinical audiences.
• Experience as medical director or monitor on oncology/hematology programs.

Responsibilities

• Author and review evaluation tasks requiring clinical judgment in oncology and hematology.
• Assess defensibility of efficacy and safety conclusions.
• Apply judgment to dose escalation, toxicity, and adverse event grading.
• Evaluate benefit-risk reasoning and management strategies.
• Identify clinically implausible content vs legitimate variation.
• Provide structured rationales for non-clinical audiences.

Skills

Clinical trials

CTCAE grading

Medical monitoring

Written communication

Oncology/Hematology

Education

Board certification in medical oncology/hematology

Job description

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.