Remote Oncology Clinical Researcher for AI Training

Alignerr Corp.; Pittsburgh (Allegheny County); Remote; USD 110,000 - 165,000; Part time

Job summary

Alignerr Corp. is seeking an Oncology Clinical Researcher for an AI training program. This fully remote, hourly contract role invites you to design trial frameworks, oversee enrollment strategies, and ensure regulatory standards are met for AI training workflows.

You will analyze cancer trial data, evaluate safety endpoints and biomarkers, and translate findings into regulatory-ready outputs compatible with FDA/EMA guidance. Collaboration is asynchronous and global.

Qualifications

• Design and evaluate oncology trial frameworks for AI training
• Analyze cancer trial data including safety, efficacy, and biomarker results
• Translate trial findings into regulatory reporting standards
• Review AI-generated oncology insights for clinical relevance and regulatory alignment
• Provide expert feedback to improve frontier AI models during training

Responsibilities

• Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance standards — for use in AI training and evaluation workflows
• Analyze cancer trial data, including safety profiles, efficacy endpoints, and biomarker results, to assess how well AI systems interpret and represent real-world treatment outcomes
• Translate trial findings into clear, structured outputs aligned with regulatory reporting standards used by agencies such as the FDA and EMA
• Review AI-generated oncology insights for clinical accuracy, scientific relevance, and regulatory alignment
• Provide expert feedback that helps frontier AI models reason more accurately about cancer research and clinical decision-making

Skills

Oncology trials design

Regulatory analysis

Data interpretation

Remote collaboration

Job description

Alignerr Corp. is seeking an Oncology Clinical Researcher for an AI training program. This fully remote, hourly contract role invites you to design trial frameworks, oversee enrollment strategies, and ensure regulatory standards are met for AI training workflows.

You will analyze cancer trial data, evaluate safety endpoints and biomarkers, and translate findings into regulatory-ready outputs compatible with FDA/EMA guidance. Collaboration is asynchronous and global.