Overview

Oncology Clinical Researcher Jobs in Indianapolis, IN at Alignerr

Title: Oncology Clinical Researcher

Company: Alignerr

Location: Indianapolis, IN

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 work alongside leading AI research teams to ensure that the systems being built to transform cancer research are grounded in accurate, regulatory-aligned, and scientifically sound clinical knowledge.

This is a fully remote, flexible contract role. No AI background needed — just deep oncology expertise and a sharp eye for clinical quality.

  • 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 validity, and regulatory alignment
  • Apply your expertise in trial design — including protocol development, patient enrollment standards, and ethical compliance — to assess and improve AI outputs
  • Analyze AI-generated interpretations of cancer trial data, including safety profiles, efficacy endpoints, and biomarker findings
  • Evaluate how well AI systems translate trial outcomes into regulatory and scientific contexts relevant to FDA/EMA standards
  • Provide structured, expert feedback that directly shapes how frontier AI models reason about real 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 command of oncology clinical data analysis — endpoints, safety profiles, biomarkers, and beyond
  • Solid familiarity with regulatory submission standards for agencies such as the FDA or EMA
  • Naturally detail-oriented with a rigorous, systematic approach to evaluating clinical information
  • Able to communicate complex clinical findings clearly and concisely in written form
  • No prior AI or tech experience required

Nice to Have

  • Prior experience with data annotation, data quality assessment, or AI evaluation workflows
  • Background in translational oncology, clinical pharmacology, or regulatory affairs
  • Experience authoring or reviewing clinical study reports, IND/NDA submissions, or publications
  • Familiarity with AI tools or clinical decision support platforms as an end user

Why Join Us

  • Work directly on frontier AI systems that are transforming how cancer research is conducted
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, high-impact project work
  • Influence how AI models understand, evaluate, and reason about real-world oncology data
  • Collaborate with world-leading AI research teams and labs
  • Potential for ongoing work and contract extension as new projects launch
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