Senior Clinical Scientist for AI Training (Remote)

Alignerr Corp.; Sheffield (TX); Remote; USD 138,000 - 248,000; Part time

Job summary

Alignerr seeks a Principal Clinical Scientist to guide AI training with senior clinical trial expertise, ensuring regulatory-grade data underpinning biomedical AI. This fully remote hourly contract role involves designing regulator-ready protocols, auditing trial results, and providing expert feedback to improve AI reasoning, on a flexible schedule.

You will interpret clinical data for regulatory standards, identify gaps in AI reasoning, and contribute to setting standards for regulatory science

Qualifications

• Senior clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission.
• Expert interpreter of clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies.
• Strong grounding in clinical research methodology, biostatistics, or translational science.
• Precise, rigorous thinker who can spot flawed reasoning or incomplete analysis quickly.
• Clear written communicator who can document feedback in structured, actionable formats.

Responsibilities

• Design and review clinical trial protocols used to generate high-quality, regulator-ready training datasets for AI systems.
• Interpret and audit clinical trial results to ensure accuracy, consistency, and alignment with regulatory standards.
• Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance.
• Identify gaps, errors, and weaknesses in how AI models reason about clinical evidence — and provide expert feedback to correct them.
• Help define what "good" looks like when AI tackles clinical trial data, outcomes, and methodology.
• Work independently and asynchronously on task-based assignments — on your own schedule.

Skills

Clinical trial design

Regulatory submission experience

Biostatistics

Clinical data interpretation

Regulatory affairs understanding

Job description

Alignerr seeks a Principal Clinical Scientist to guide AI training with senior clinical trial expertise, ensuring regulatory-grade data underpinning biomedical AI. This fully remote hourly contract role involves designing regulator-ready protocols, auditing trial results, and providing expert feedback to improve AI reasoning, on a flexible schedule.

You will interpret clinical data for regulatory standards, identify gaps in AI reasoning, and contribute to setting standards for regulatory science