Oncology Clinical Researcher

Alignerr Corp.; France; Remote; EUR 14,000 - 55,000; Part time

Benefits offered by this job

Remote work

Flexible schedule

Freelance autonomy

Job summary

Alignerr is seeking an experienced Oncology Clinical Researcher to bring real-world clinical rigor to AI training in oncology. You’ll design and evaluate trial protocols, analyze endpoints, and ensure regulatory alignment across FDA/EMA submissions, while evaluating AI-generated insights for scientific validity.

You’ll work fully remotely on a flexible, hourly contract, collaborating with leading AI teams and contributing on your own schedule to high-impact cancer research initiatives.

Qualifications

• Experience in designing and managing oncology clinical trials from protocol development through data readout.
• Strong ability to analyze oncology clinical data including endpoints, safety and biomarkers.
• Familiarity with regulatory submission standards (FDA/EMA) for oncology trials.

Responsibilities

• Design and evaluate oncology trial protocols with study design, enrollment framing, and regulatory/ethical compliance.
• Analyze cancer trial data across safety, efficacy, and biomarker endpoints to assess performance.
• Translate trial outcomes into regulatory-grade scientific narratives aligned with agency standards.
• Review AI-generated oncology content for scientific accuracy, regulatory alignment, and real-world applicability.
• Help shape how frontier AI systems understand, reason about, and communicate oncology concepts.
• Work independently and asynchronously on assigned tasks.

Skills

Oncology trial design

Data analysis

Regulatory submissions

Independent work

AI evaluation

Job description

Oncology Clinical Researcher (AI Training)

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 save lives at scale?

About The Role

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 the oncology data, insights, and reasoning powering next‑generation AI models meet the highest scientific, regulatory, and clinical standards.

This is a fully remote, flexible contract role — built for working clinicians, researchers, and oncology experts who want to contribute to something genuinely transformative 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 protocols — including study design, patient enrollment frameworks, and regulatory and ethical compliance standards
• Analyze cancer trial data across safety, efficacy, and biomarker endpoints to assess treatment performance and clinical relevance
• Translate trial outcomes into regulatory‑grade scientific narratives aligned with FDA, EMA, and other agency submission standards
• Review and evaluate AI‑generated oncology content and clinical insights for scientific accuracy, regulatory alignment, and real‑world clinical applicability
• Help shape how frontier AI systems understand, reason about, and communicate complex oncology concepts
• 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, biomarkers, and statistical outcomes
• Familiar with regulatory submission standards for agencies such as the FDA or EMA
• Detail‑oriented and rigorous — you hold AI‑generated content to the same standards you'd apply in a clinical or regulatory setting
• Comfortable working independently on structured, task‑based assignments

Nice to Have

• Prior experience with data annotation, data quality review, or AI evaluation workflows
• Background in oncology drug development, translational research, or clinical operations
• Experience authoring or reviewing clinical study reports, regulatory briefing documents, or scientific publications
• Familiarity with AI tools or content evaluation platforms

Why Join Us

• Work directly on frontier AI systems transforming cancer research and oncology medicine
• Fully remote and flexible — contribute on your own schedule, from anywhere
• Freelance autonomy with the structure of meaningful, high‑impact work
• Collaborate with world‑class AI research labs on problems that matter
• Influence how AI models understand and reason about real oncology data at a foundational level
• Potential for ongoing work and contract extension as new projects launch