Senior Clinical Scientist — AI Training (Remote)

Alignerr Corp.

Pittsburgh (Allegheny County)

On-site

USD 138,000 - 248,000

Part time

34 hours ago
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Job summary

Alignerr is seeking a Principal Clinical Scientist to shape how real-world clinical data informs AI training and evaluation. This fully remote hourly contract role demands senior clinical expertise and regulatory acumen to ensure regulator-ready datasets.

You will design protocols, audit trial results, and assess AI-generated analyses for regulatory relevance, collaborating with world-leading AI teams. Flexible, asynchronous work supports experts who value rigorous science and impactful

Qualifications

  • Senior clinical professional with hands-on experience designing clinical trial protocols for regulatory submission.
  • Deep expertise interpreting clinical data for major regulatory agencies such as the FDA, EMA, or equivalent bodies.
  • Strong grounding in clinical research methodology, biostatistics, or translational science.
  • Detail-oriented and rigorous — you hold data to the highest standards of accuracy and scientific integrity.
  • Comfortable working independently and asynchronously in a remote, task-based environment.

Responsibilities

  • Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets for AI training and evaluation
  • 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
  • Provide expert feedback that directly shapes how AI models reason about clinical trial data, outcomes, and methodology
  • Apply your regulatory expertise — FDA, EMA, or equivalent — to validate the integrity of clinical data used in AI systems

Skills

Clinical trial design
Regulatory submissions
Biostatistics
FDA/EMA knowledge
Data interpretation

Tools

Clinical NLP tools
AI platforms

Job description

Alignerr is seeking a Principal Clinical Scientist to shape how real-world clinical data informs AI training and evaluation. This fully remote hourly contract role demands senior clinical expertise and regulatory acumen to ensure regulator-ready datasets.

You will design protocols, audit trial results, and assess AI-generated analyses for regulatory relevance, collaborating with world-leading AI teams. Flexible, asynchronous work supports experts who value rigorous science and impactful

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