Oncology Clinical Researcher

Alignerr Corp.; Viseu; Remote; EUR 55,000 - 110,000; Part time

Job summary

Alignerr Corp. is seeking an Oncology Clinical Researcher to guide AI training with real-world regulatory and clinical insights. You will evaluate AI-generated oncology content to ensure it reflects FDA/EMA standards and trial design rigor.

This fully remote contract offers 10–40 hours per week, leveraging your expertise in endpoints, safety, and biomarkers to shape how AI models reason about oncology data. Work independently within a cutting-edge AI research environment.

Qualifications

• Designing and managing oncology trials from protocol through data readout.
• Strong analytical background in oncology endpoints, safety, and biomarkers.
• Familiar with FDA/EMA regulatory submission standards.

Responsibilities

• Review and evaluate AI-generated oncology content for accuracy and regulatory alignment.
• Apply trial design expertise to assess AI outputs related to study protocols, enrollment frameworks, and compliance standards.
• Provide structured feedback to shape how frontier AI models understand and communicate oncology knowledge.
• Work independently and asynchronously on your own schedule.

Skills

Oncology trials

Clinical data analysis

Regulatory submissions

Documentation

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 research that may one day save millions of lives? We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll evaluate and inform AI-generated oncology content, ensuring the systems being built today reflect genuine regulatory, scientific, and clinical standards.

This is a fully remote, flexible contract role built for seasoned oncology professionals who want to make an impact beyond the clinic. 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 to assess AI outputs related to study protocols, patient enrollment frameworks, and compliance standards Analyze AI-generated interpretations of cancer trial data — including safety profiles, efficacy endpoints, and biomarker results — and flag errors or gaps Evaluate the quality of AI-produced regulatory and scientific content against real-world FDA/EMA submission standards Provide structured, expert feedback that directly shapes how frontier AI models understand and communicate oncology knowledge 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 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 systematic — you notice when something doesn't meet the clinical or scientific bar Clear and concise written communicator who can document feedback effectively Comfortable working independently without hand-holding

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 peer-reviewed publications or regulatory dossiers Familiarity with AI tools or content evaluation platforms

Why Join Us

Work directly on frontier AI systems that are transforming how cancer research is understood and advanced 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 reason about real oncology data — your clinical judgment shapes the science Collaborate with world-leading AI research teams and labs Potential for ongoing work and contract extension as new projects launch

Oncology Clinical Researcher Portalegre, Portuguese Republic, PT