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Oncology Clinical Researcher

Job in Sheffield, Pecos County, Texas, 79781, USA
Listing for: Alignerr Corp.
Full Time position
Listed on 2026-10-01
Job specializations:
  • IT/Tech
  • Research/Development
Salary/Wage Range or Industry Benchmark: 83000 - 124000 USD Yearly USD 83000.00 124000.00 YEAR
Job Description & How to Apply Below
Location: Sheffield

Oncology Clinical Researcher (AI Training)
About The Role

What if your deep knowledge of cancer clinical trials could directly shape how AI understands and reasons about oncology — influencing the next generation of tools used by researchers, clinicians, and drug developers worldwide?

We're looking for Oncology Clinical Researchers to bring real-world trial expertise into AI-driven workflows. You'll review, evaluate, and inform the AI systems being built to support cancer research — ensuring they reflect the rigor, regulatory standards, and clinical nuance that this field demands.

This is a fully remote, flexible contract role designed for experienced oncology professionals who want to do meaningful work on their own schedule.

  • Organization:
    Alignerr
  • Type:
    Hourly Contract
  • Location:

    Remote
  • Commitment: 10–40 hours/week
What You'll Do
  • Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment logic, and regulatory compliance standards — to ensure AI-generated outputs meet real-world clinical expectations
  • Analyze cancer trial data across safety, efficacy, and biomarker dimensions to assess the accuracy and clinical relevance of AI outputs
  • Translate trial outcomes and findings into clear, structured evaluations aligned with FDA, EMA, and international regulatory standards
  • Review AI-generated clinical insights and flag errors in scientific reasoning, data interpretation, or regulatory alignment
  • Provide expert feedback that directly shapes how frontier AI models understand oncology research
Who You Are
  • Experienced in designing and managing oncology clinical trials — from protocol development through data readout
  • Strong command of oncology data analysis, including clinical endpoints, safety profiles, and biomarker interpretation
  • Familiar with regulatory submission standards for agencies such as the FDA or EMA
  • Detail-oriented and capable of evaluating complex clinical information with precision
  • Comfortable working independently and asynchronously in a remote environment
Nice to Have
  • Prior experience with data annotation, data quality review, or AI evaluation workflows
  • Background in translational oncology or drug development
  • Experience contributing to publications, regulatory submissions, or clinical decision-support tools
Why Join Us
  • Work directly on frontier AI systems that are transforming how the world approaches cancer research
  • Fully remote and flexible — structure your hours around your life, not the other way around
  • Freelance autonomy with the depth of meaningful, expert-level work
  • Collaborate with world-leading AI research teams and labs on problems that matter
  • Influence how AI models reason about real oncology data — your expertise sets the standard
  • Potential for ongoing work and contract extension as new projects launch
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