Clinician

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This is a fully remote position open to candidates based in United States.

Pay: $160$200/hr

Role Title: Clinician (Oncology / Hematology)

Role Type: Contractor

Location: Remote

We are engaging Clinician (Oncology / Hematology)s to contribute to a customers project at the forefront of AI in this role youll apply your 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 domain knowledge is what matters.

Scope of Work

1. Author and review evaluation tasks that require nuanced clinical judgment leveraging Clinical Study Reports periodic safety reports and regulatory correspondence in oncology and haematology.
2. Assess the clinical defensibility of efficacy and safety conclusions ensuring endpoints and effect sizes reflect true clinical significance.
3. Apply advanced judgment to dose escalation dose-limiting toxicity modifications adverse event grading and attribution and the coherence of patient narratives.
4. Evaluate benefit-risk reasoning scrutinizing the durability of conclusions in light of new events and the realism of described management strategies.
5. Identify and flag content that is clinically implausible or internally inconsistent distinguishing these from legitimate clinical variation.
6. Provide structured guideline-based written rationales that clearly explain the validity or limitations of clinical interpretations for a non-clinical audience.

Preferred Qualifications

1. Specialist registration or board certification in medical oncology and/or haematology with 5 years of post-training clinical experience.
2. Direct involvement in clinical trials as investigator sub-investigator or sponsor-side medical monitor safety physician or clinical development physician.
3. Proficiency with CTCAE grading relevant response criteria (RECIST Lugano IMWG IWCLL ELN) and outcome endpoints (ORR DoR PFS OS MRD).
4. Hands-on experience with trial documents such as protocols investigator brochures CSRs safety narratives or DSMB/IDMC materials.
5. Demonstrated excellence in written communication with clear structured explanations of clinical reasoning tailored for non-clinical readers.
6. Previous roles in medical monitoring or as medical director on oncology or haematology programmes and committee participation (IDMC DSMB adjudication or independent review committees).
7. Peer-reviewed publication record or authorship on clinical trial manuscripts with any exposure to AI-assisted clinical review tools seen as a plus.

How to apply

Apply here with your profile. We will then email you a link to complete your application on the hiring platform your application is only considered once that final step is done.