Back to remote jobs

Oncology Clinical Researcher

Alignerr

AI Expert - Clinical & Medical Contractor
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 the next generation of tools used by researchers, clinicians, and regulators worldwide?

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 interpret oncology trial data — ensuring the science is accurate, the regulatory grounding is solid, and the clinical reasoning actually holds up.

This is a fully remote, flexible contract role built for clinical 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

  • Review and evaluate AI-generated oncology content for clinical accuracy, regulatory alignment, and scientific validity
  • Apply your trial design expertise to assess AI outputs related to study protocols, patient enrollment, endpoint selection, and compliance standards
  • Analyze AI interpretations of cancer trial data — including safety profiles, efficacy outcomes, and biomarker results — and flag errors or gaps
  • Evaluate how well AI-generated insights reflect real-world regulatory standards for agencies such as the FDA and EMA
  • Translate your clinical and scientific judgment into structured, actionable feedback that directly improves AI model training
  • Work independently and asynchronously on task-based assignments — fully on your own schedule

Who You Are

  • Experienced in designing and managing oncology clinical trials, from protocol development through data readout
  • Strong command of oncology clinical data analysis — including endpoints, safety profiles, and biomarkers
  • Familiar with regulatory submission standards for agencies such as the FDA or EMA
  • Detail-oriented and rigorous — you notice when clinical reasoning doesn't hold up
  • Able to communicate complex scientific assessments clearly in writing
  • Comfortable working independently without hand-holding

Nice to Have

  • Prior experience with data annotation, data quality review, or AI evaluation workflows
  • Background in oncology drug development, translational research, or regulatory affairs
  • Experience writing or reviewing clinical study reports, protocols, or regulatory submissions
  • Familiarity with AI tools or content evaluation platforms as an end user

Why Join Us

  • Work directly on frontier AI systems that are transforming how cancer research is understood and applied
  • Influence how AI models reason about real oncology data — your expertise shapes the science
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, task-based work
  • Collaborate with world-leading AI research teams and labs
  • Potential for ongoing work and contract extension as new projects launch
Apply now

You will be redirected to the company's website to complete your application.

Apply now

Stay in the loop.

One email per week, 5 hand-picked roles.