Oncology Clinical Researcher
Boston, MA
Contract
Remote
1 month ago
About the role
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.
What You'll Do
Who You Are
Nice to Have
Why Join Us
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
Skills
Technology, Information and Internet