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Oncology Clinical Researcher

Alignerr
Department:Data Analysis
Type:REMOTE
Region:Australia
Location:Sydney, New South Wales, Australia
Experience:Mid-Senior level
Estimated Salary:A$80,000 - A$120,000
Skills:
ONCOLOGY CLINICAL TRIALSPROTOCOL DEVELOPMENTPATIENT ENROLLMENTREGULATORY COMPLIANCEFDA STANDARDSEMA STANDARDSDATA ANALYSISBIOMARKERSCLINICAL DATA REVIEW
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Job Description

Posted on: July 2, 2026

Oncology Clinical Researcher (AI Training)About The Role What if your deep expertise in cancer clinical trials could directly shape how AI reasons about oncology — influencing the tools that researchers, clinicians, and scientists rely on worldwide? We're looking for Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll evaluate, review, and improve AI-generated oncology content — ensuring it meets the scientific, regulatory, and clinical standards that matter most in cancer research. This is a fully remote, flexible contract role built for experienced oncology professionals. No AI background required — just deep knowledge of cancer clinical trials and a sharp eye for accuracy.

  • 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, and compliance — to assess AI outputs against real-world standards
  • Analyze AI-generated interpretations of cancer trial data, including efficacy, safety, and biomarker findings
  • Evaluate the quality of AI-produced regulatory and scientific documentation against FDA/EMA submission standards
  • Provide structured, expert feedback that directly improves how AI models understand and reason about oncology
  • 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 oncology clinical data — including endpoints, safety profiles, and biomarkers
  • Familiar with regulatory submission standards for agencies such as the FDA or EMA
  • Detail-oriented with a systematic, thorough approach to evaluating complex scientific content
  • Able to communicate expert feedback clearly and concisely in written form
  • No prior AI or tech experience required

Nice to Have

  • Prior experience with data annotation, data quality assurance, or AI evaluation workflows
  • Background in translational oncology or biomarker-driven research
  • Experience contributing to publications, clinical study reports, or regulatory dossiers
  • Familiarity with AI tools or clinical decision-support platforms as an end user

Why Join Us

  • Work directly on frontier AI systems transforming the future of cancer research
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, expert-driven work
  • Influence how AI models understand, interpret, and communicate real oncology science
  • Potential for ongoing work and contract extension as new projects launch
  • Collaborate with world-leading AI research teams and labs on high-impact projects
Originally posted on LinkedIn

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