Principal Clinical Scientist
Alignerr · Seattle, WA · Today
RemoteRemoteAnalystContract
What You'll Do
- 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 regulatory relevance
- Evaluate AI-generated clinical analyses for scientific soundness and alignment with FDA, EMA, or equivalent regulatory expectations
- Provide structured expert feedback that directly improves how AI models reason about clinical trial data, endpoints, and outcomes
- Help establish the standard for how clinical evidence is represented, evaluated, and used within advanced AI systems
Who You Are
- Senior clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission
- Strong expertise interpreting clinical data for regulatory agencies such as the FDA, EMA, or equivalent bodies
- Precise, detail-oriented communicator — able to articulate complex scientific reasoning clearly and consistently
- Self-directed and comfortable working independently on structured, task-based assignments
Nice to Have
- Prior experience with data annotation, data quality evaluation, or AI evaluation workflows
- Background in pharmacovigilance, outcomes research, or evidence-based medicine
- Familiarity with AI tools or clinical decision-support systems as an end user