Oncology Clinical Researcher

Alignerr Corp.; Boston (MA); Remote; USD 110,000 - 165,000; Full time

Job summary

Alignerr is seeking an experienced Oncology Clinical Researcher to shape how AI systems interpret oncology trial data. This fully remote, hourly contract role offers a senior professional the freedom to contribute rigorously on their own schedule, with a focus on regulatory alignment and scientific accuracy.

The role emphasizes designing trial frameworks, data interpretation, and translating outcomes into regulatory narratives for FDA/EMA contexts.

Qualifications

• Experience designing and managing oncology clinical trials from protocol to data readout.
• Strong analytical background in oncology trial data including endpoints and biomarkers.
• Familiarity with FDA/EMA submission standards.
• Detail-oriented and scientifically rigorous in AI-driven research contexts.

Responsibilities

• Design and evaluate oncology trial frameworks including study protocols and enrollment strategies.
• Analyze trial data for safety, efficacy endpoints, and biomarkers.
• Translate trial outcomes into regulatory and scientific narratives aligned with submission standards.
• Review AI-generated oncology insights for clinical accuracy and regulatory soundness.
• Help establish quality benchmarks for AI models interpreting real-world oncology research.
• Work independently and asynchronously on your schedule.

Skills

Oncology clinical trial design

Data analysis

Regulatory submissions

Scientific writing

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 regulatory teams worldwide?

We're looking for experienced Oncology Clinical Researchers to bring real-world scientific rigor into AI-driven research workflows. You'll evaluate, guide, and improve how frontier AI systems interpret oncology trial data — ensuring the insights they generate meet the standards of actual clinical and regulatory practice.

This is a fully remote, flexible contract role built for senior oncology professionals who want to contribute to something genuinely consequential — 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 strategies, and regulatory compliance standards
• Analyze cancer trial data covering safety profiles, efficacy endpoints, and biomarker results to assess treatment performance
• Translate trial outcomes into clear regulatory and scientific narratives aligned with FDA/EMA submission standards
• Review and critique AI-generated oncology insights for clinical accuracy, scientific relevance, and regulatory soundness
• Help establish the quality benchmarks that define how AI models understand real-world oncology research
• 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 analytical background in oncology clinical data, including endpoints, safety profiles, and biomarkers
• Familiar with regulatory submission standards for agencies such as the FDA or EMA
• Detail-oriented and scientifically rigorous — you hold AI-generated content to the same standards you'd apply in a clinical or regulatory setting
• Able to communicate complex oncology concepts clearly and precisely in writing
• 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, clinical pharmacology, or biomarker science
• Experience contributing to peer-reviewed publications or regulatory submissions
• Familiarity with AI tools or clinical decision-support systems

Why Join Us

• Work directly on frontier AI systems being built to transform cancer research and clinical decision-making
• Influence how the next generation of AI understands real oncology data — at the protocol, endpoint, and regulatory level
• Fully remote and flexible — work when and where it suits you
• Freelance autonomy with the structure of meaningful, high-impact work
• Collaborate with leading AI research labs and teams at the cutting edge of medical AI
• Potential for ongoing work and contract extension as new projects launch