Job Title
Clinician (Oncology / Hematology) - AI Trainer
Job Type
Contractor
Compensation Structure
Compensation is hourly. The hourly rate will be determined based on experience, qualifications, and project requirements.
Location
Remote
Job Summary
In this role, you'll apply your clinical expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input.
No prior experience in AI is required—your expertise in oncology and hematology is what matters most.
You'll contribute to the development of AI systems by evaluating complex clinical content, applying evidence-based medical judgment, and reviewing oncology and hematology documentation used in clinical research and regulatory submissions.
Key Responsibilities
- Author and review evaluation tasks based on Clinical Study Reports (CSRs), periodic safety reports, and regulatory documentation in oncology and hematology.
- Assess the clinical validity of efficacy and safety conclusions, ensuring endpoints and effect sizes accurately reflect clinical significance.
- Evaluate dose escalation strategies, dose-limiting toxicities, treatment modifications, adverse event grading, attribution, and patient narratives.
- Review benefit-risk assessments and determine whether conclusions remain appropriate as new clinical evidence emerges.
- Identify clinically implausible or internally inconsistent content while distinguishing them from legitimate clinical variation.
- Provide structured, guideline-based written rationales that clearly explain clinical reasoning for technical and non-technical audiences.
Required Skills and Qualifications
- Board certification or specialist registration in Medical Oncology and/or Hematology.
- Minimum of 5 years of post-training clinical experience.
- Direct experience participating in clinical trials as an investigator, sub-investigator, sponsor-side medical monitor, safety physician, or clinical development physician.
- Strong knowledge of CTCAE grading, RECIST, Lugano, IMWG, IWCLL, ELN response criteria, and clinical endpoints including ORR, DoR, PFS, OS, and MRD.
- Hands-on experience with clinical trial documents such as protocols, investigator brochures, Clinical Study Reports (CSRs), safety narratives, or DSMB/IDMC materials.
- Excellent written and verbal communication skills with the ability to clearly explain complex clinical concepts to diverse audiences.
Preferred Qualifications
- Previous experience serving as a Medical Monitor or Medical Director for oncology or hematology programs.
- Participation in IDMC, DSMB, adjudication committees, or independent review committees.
- Peer-reviewed publications or authorship of clinical trial manuscripts.
- Familiarity with AI-assisted clinical review tools or AI-supported medical documentation workflows.
Start Timeline & Availability
We typically fill roles within 48 hours and are looking for professionals ready to begin quickly. If selected, you'll be expected to start your first tasks within 24–48 hours after completing onboarding.
Job Type: Contract
Pay: $160.00 - $200.00 per hour
Benefits:
Work Location: Remote
