Oncology Clinical Researcher

About The Role

Imagine using your specialized expertise in oncology clinical trials to directly influence AI systems that interpret and reason about one of the most intricate areas in medicine. We seek Oncology Clinical Researchers to lend scientific precision and clinical insight to pioneering AI projects, ensuring these models are built on accurate and trustworthy oncology knowledge.

This position is a fully remote, flexible contract opportunity aimed at seasoned oncology professionals wishing to engage in advanced AI research while remaining connected to their clinical specialty.

Organization: Alignerr
Type: Hourly Contract
Location: Remote
Commitment: 10–40 hours weekly

Key Responsibilities

• Critically review AI-generated oncology content for clinical correctness, scientific integrity, and adherence to regulatory guidelines.
• Utilize your knowledge of clinical trial design, including protocol crafting, patient recruitment, and endpoint determination, to evaluate AI's representation of real-world oncology standards.
• Interpret oncology trial data outputs such as safety assessments, efficacy outcomes, and biomarker analysis to identify inaccuracies or shortcomings in AI conclusions.
• Assess AI-origin regulatory and scientific documentation for compliance with FDA, EMA, and ICH standards.
• Deliver detailed, expert feedback to refine AI understanding of oncology data and clinical decision processes.
• Operate independently and asynchronously, managing your schedule fully.

Candidate Profile

• Proven experience in the design and administration of oncology clinical trials from initial protocol development through final data reporting.
• Strong analytical expertise in oncology clinical datasets, including interpretation of trial endpoints, safety profiles, and biomarker data.
• Knowledgeable about regulatory submission requirements for major agencies such as FDA and EMA.
• Highly detail-focused with a systematic approach to examining complex scientific material.
• Capable of working solo in a remote, task-oriented setting.

Additional Desirable Qualifications

• Experience in data annotation, quality assessment, or AI evaluation methodologies.
• A background in translational oncology or clinical and regulatory writing.
• Familiarity with biomarker-targeted trial design or precision oncology concepts.
• Experience using AI tools or content evaluation platforms.

Why This Role

• Contribute directly to state-of-the-art AI systems revolutionizing cancer research.
• Shape how next-generation AI models incorporate genuine oncology clinical data and regulatory practices.
• Enjoy a fully remote, flexible working arrangement adapting to your lifestyle.
• Benefit from the independence of freelance work combined with meaningful, expert-driven projects.
• Collaborate alongside top-tier AI research groups and laboratories.
• Opportunities for continued engagement and contract renewal with emerging projects.