Clinical Systems Analyst (AI Training) About the Role At Alignerr, we partner with the world's leading AI research teams and labs to build and train cutting-edge AI models.
Oncology Clinical Researcher
Remote (Global)
$40 – $80/hr
June 22, 2026
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 transform how cancer is diagnosed and treated?
We're looking for experienced Oncology Clinical Researchers to bring rigorous, real-world clinical trial knowledge into cutting-edge AI development workflows. You'll review, evaluate, and inform AI-generated oncology content — ensuring it reflects the scientific, regulatory, and clinical standards that matter in practice.
This is a fully remote, flexible contract role built for working oncology researchers and clinical scientists who want to engage with frontier AI on their own terms.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
What You'll Do
- Evaluate AI-generated oncology content for clinical accuracy, scientific rigor, and regulatory alignment
- Apply your expertise in study protocol design, patient enrollment standards, and trial oversight to assess AI outputs against real-world best practices
- Analyze and interpret cancer trial data — including safety profiles, efficacy endpoints, and biomarker results — to identify errors or gaps in AI reasoning
- Review AI-generated regulatory and scientific content for alignment with FDA, EMA, and international submission standards
- Provide structured, expert feedback that directly improves how AI models understand and generate oncology knowledge
- 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 background in analyzing clinical trial data, including primary and secondary endpoints, safety reporting, and biomarker analysis
- Familiar with regulatory submission standards and documentation requirements for agencies such as the FDA or EMA
- Detail-oriented and rigorous — you hold AI outputs to the same standards you'd apply in a real clinical or regulatory setting
- Able to communicate complex clinical findings clearly in written feedback
- Self-motivated and comfortable working independently in a remote, asynchronous environment
Nice to Have
- Prior experience with data annotation, evaluation systems, or AI quality workflows
- Background in translational oncology, biostatistics, or clinical pharmacology
- Experience authoring or reviewing regulatory submissions, clinical study reports, or scientific publications
- Familiarity with AI tools or clinical decision support systems
Why Join Us
- Work directly on frontier AI systems being developed alongside the world's leading AI research labs
- Fully remote and flexible — work when and where it suits you, on a schedule you control
- Freelance autonomy with the substance of meaningful, high-impact work
- Contribute to AI that could reshape how cancer research is conducted and communicated at a global scale
- Potential for ongoing work and contract extension as new oncology AI projects launch
Apply now
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