Oncology Clinical Researcher
Alignerr · Adelaide, South Australia, Australia
FLEXTIME
Remote
Posted Oct 12, 2026
40 - 80 USD / hour
Job Description
**Oncology Clinical Researcher (AI Training)** **About The Role** What if your deep expertise in cancer clinical trials could directly shape how AI understands and reasons about oncology --- influencing research that could one day impact millions of patients?
We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll evaluate, guide, and improve how advanced AI systems handle oncology trial data, regulatory standards, and clinical decision-making --- ensuring the science is right.
This is a fully remote, flexible contract role built for oncology professionals who want to contribute to something genuinely frontier --- on their own schedule.
* Organization: Alignerr
* Type: Hourly Contract
* Location: Remote
* Commitment: 10--40 hours/week
**What You'll Do**
* Review and evaluate AI-generated oncology content for clinical accuracy, scientific rigor, and regulatory alignment
* Apply your expertise in clinical trial design --- including protocol development, patient enrollment, and compliance standards --- to assess AI outputs
* Analyze AI-generated interpretations of cancer trial data, including safety profiles, efficacy endpoints, and biomarker results
* Evaluate the quality and accuracy of AI-produced regulatory and scientific reporting against FDA/EMA submission standards
* Provide structured, expert feedback that directly shapes how AI models understand real-world oncology data
* Work independently and asynchronously --- fully on your own schedule
**Who You Are**
* Experienced in designing and managing oncology clinical trials from protocol development through data readout
* Strong analytical background in oncology clinical data --- endpoints, safety profiles, and biomarkers
* Familiar with regulatory submission standards for agencies such as the FDA or EMA
* Detail-oriented and capable of translating deep clinical knowledge into clear, structured evaluation
* Comfortable working independently without close supervision
**Nice to Have**
* Prior experience with data annotation, data quality assurance, or AI evaluation workflows
* Background in translational oncology or biomarker research
* Experience contributing to peer-reviewed publications or regulatory dossiers
* Familiarity with AI tools or clinical informatics platforms
**Why Join Us**
* Work directly on frontier AI systems being built alongside the world's leading AI research labs
* Shape how AI models reason about real oncology science --- your expertise has direct, tangible impact
* Fully remote and flexible --- work when and where it suits you
* Freelance autonomy with the intellectual depth of meaningful, high-stakes scientific work
* Potential for ongoing work and contract extension as new projects launch
* Collaborate with a global network of domain experts pushing the boundaries of AI in medicine
We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll evaluate, guide, and improve how advanced AI systems handle oncology trial data, regulatory standards, and clinical decision-making --- ensuring the science is right.
This is a fully remote, flexible contract role built for oncology professionals who want to contribute to something genuinely frontier --- on their own schedule.
* Organization: Alignerr
* Type: Hourly Contract
* Location: Remote
* Commitment: 10--40 hours/week
**What You'll Do**
* Review and evaluate AI-generated oncology content for clinical accuracy, scientific rigor, and regulatory alignment
* Apply your expertise in clinical trial design --- including protocol development, patient enrollment, and compliance standards --- to assess AI outputs
* Analyze AI-generated interpretations of cancer trial data, including safety profiles, efficacy endpoints, and biomarker results
* Evaluate the quality and accuracy of AI-produced regulatory and scientific reporting against FDA/EMA submission standards
* Provide structured, expert feedback that directly shapes how AI models understand real-world oncology data
* Work independently and asynchronously --- fully on your own schedule
**Who You Are**
* Experienced in designing and managing oncology clinical trials from protocol development through data readout
* Strong analytical background in oncology clinical data --- endpoints, safety profiles, and biomarkers
* Familiar with regulatory submission standards for agencies such as the FDA or EMA
* Detail-oriented and capable of translating deep clinical knowledge into clear, structured evaluation
* Comfortable working independently without close supervision
**Nice to Have**
* Prior experience with data annotation, data quality assurance, or AI evaluation workflows
* Background in translational oncology or biomarker research
* Experience contributing to peer-reviewed publications or regulatory dossiers
* Familiarity with AI tools or clinical informatics platforms
**Why Join Us**
* Work directly on frontier AI systems being built alongside the world's leading AI research labs
* Shape how AI models reason about real oncology science --- your expertise has direct, tangible impact
* Fully remote and flexible --- work when and where it suits you
* Freelance autonomy with the intellectual depth of meaningful, high-stakes scientific work
* Potential for ongoing work and contract extension as new projects launch
* Collaborate with a global network of domain experts pushing the boundaries of AI in medicine
Additional Details
- City
- Adelaide
- State
- South Australia
- Country
- au
- Industry
- IT
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