Oncology Clinical Researcher

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 affects millions of patients worldwide
Were looking for Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. Youll work alongside leading AI research teams to ensure that the oncology knowledge embedded in frontier AI systems reflects genuine regulatory, scientific, and clinical standards.
This is a fully remote, flexible contract role built for experienced oncology professionals who want to extend their impact beyond the clinic.

• Organization: Alignerr
• Type: Hourly Contract
• Location: Remote
• Commitment: 10–40 hours/week
  

What Youll Do

• Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance considerations
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  Analyze cancer trial data across safety, efficacy, and biomarker endpoints to assess treatment performance and scientific validity
• Translate complex trial outcomes into clear regulatory and scientific narratives aligned with FDA/EMA submission standards
• Review and critique AI-generated oncology insights for clinical accuracy, scientific relevance, and regulatory alignment
• Help establish the standard for how AI models reason about real-world oncology data
  

Who You Are

• Experienced in designing and managing oncology clinical trials — from protocol development through data readout
• Strong analytical background in oncology clinical data, including endpoints, safety profiles, and biomarker interpretation
• Solid familiarity with regulatory submission standards for agencies such as the FDA or EMA
• Detail-oriented and comfortable applying scientific judgment in an independent, asynchronous work environment
• Motivated by the opportunity to influence how AI understands cancer research
  

Nice to Have

• Prior experience with data annotation, data quality review, or AI evaluation workflows
• Background in translational oncology or biomarker-driven trial design
• Experience preparing or reviewing regulatory submission documents (IND, NDA, BLA, or equivalent)
• Familiarity with AI tools or clinical decision-support systems
  

Why Join Us

• Work directly on frontier AI systems that are transforming how cancer research is conducted and understood
• Influence how AI models interpret and reason about real oncology data — a genuinely rare opportunity
• Fully remote and flexible — work on your own schedule, from anywhere
• Freelance autonomy with the structure of meaningful, high-impact project work
• Collaborate with world-leading AI research labs and oncology professionals globally
• Potential for ongoing work and contract extension as new projects launch