Live opening · Posted 6 days ago

Oncology Clinical Researcher

Alignerr · Seattle, WA (Remote)
Linkedin Yes
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At a glance

The key details from the original listing.

Posted 6 days ago
CompanyAlignerr
LocationSeattle, WA (Remote)
Salary$40/hr - $80/hr
Work modeYes
SourceLinkedin
Listed6 days ago

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About the role

Description supplied by the original job listing.

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 systems that may one day transform how cancer is diagnosed and treated?
We're looking for Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll review, evaluate, and inform AI-generated oncology content — ensuring it meets the scientific, regulatory, and clinical standards that matter in the real world.
This is a fully remote, flexible contract role built 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
Evaluate AI-generated clinical insights for oncology accuracy, regulatory alignment, and scientific validity
Apply your expertise in trial design — protocols, patient enrollment, compliance, and regulatory standards — to assess AI outputs
Review cancer trial data interpretations, including safety profiles, efficacy analyses, and biomarker findings
Identify gaps or errors in how AI systems represent oncology concepts, clinical methodology, and trial outcomes
Provide structured, expert-level feedback that directly shapes how frontier AI models reason about cancer research
Work independently and asynchronously 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 — endpoints, safety profiles, biomarkers, and treatment outcomes
Familiar with regulatory submission standards for agencies such as the FDA or EMA
Detail-oriented and able to provide precise, well-reasoned written feedback
Self-motivated and reliable when working independently
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 contributing to FDA/EMA submissions, clinical publications, or regulatory affairs
Familiarity with AI tools or clinical decision-support systems
Why Join Us
Work directly on frontier AI systems being built to transform cancer research
Fully remote and flexible — work when and where it suits you
Freelance autonomy with the structure of meaningful, expert-level work
Influence how AI models understand real oncology data at a foundational level
Collaborate with world-leading AI research teams and labs
Potential for ongoing work and contract extension as new projects launch

Work arrangement
Yes

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