Remote Oncology Clinical Researcher for AI Training

Alignerr Corp.; United Kingdom; Remote; GBP 103,000 - 165,000; Part time

Job summary

Alignerr Corp. is seeking an Oncology Clinical Researcher to review and improve AI-generated oncology content for clinical accuracy and regulatory compliance.

You will apply your trial-design expertise to assess real-world methodologies and analyze trial data while ensuring alignment with FDA/EMA standards. The role is fully remote, flexible, and freelance, allowing you to set your own schedule and work across global teams.

Qualifications

• Experience designing and managing oncology trials from protocol development through data readout.
• Strong background in analyzing oncology clinical data—endpoints, safety profiles, biomarkers, and statistical outputs.
• Familiarity with regulatory standards for agencies such as the FDA or EMA.
• Detail-oriented and methodical, able to translate complex clinical knowledge into clear evaluations.

Responsibilities

• Review and evaluate AI-generated oncology content for clinical accuracy, scientific validity, and regulatory alignment.
• Apply expertise in clinical trial design to assess how well AI systems understand real-world trial methodology.
• Analyze AI outputs related to cancer trial data, including efficacy results, safety profiles, and biomarker findings.
• Evaluate AI-generated regulatory and scientific content against FDA/EMA submission standards.
• Provide structured, expert feedback that shapes how AI models reason about oncology.
• Work independently and asynchronously — fully on your own schedule.

Skills

Oncology trials

Trial design

Regulatory standards

Biomarkers analysis

FDA EMA submissions

Structured feedback

Independent remote work

Tools

Data annotation workflows

AI evaluation workflows

Job description

Alignerr Corp. is seeking an Oncology Clinical Researcher to review and improve AI-generated oncology content for clinical accuracy and regulatory compliance.

You will apply your trial-design expertise to assess real-world methodologies and analyze trial data while ensuring alignment with FDA/EMA standards. The role is fully remote, flexible, and freelance, allowing you to set your own schedule and work across global teams.