Principal Clinical Scientist (AI Training)
What if your years of clinical trial expertise could directly influence how AI reasons about medical evidence, regulatory submissions, and patient outcomes? We're looking for a Principal Clinical Scientist to bring senior-level rigor to AI-driven research workflows — ensuring the clinical data that trains and evaluates next-generation AI systems meets the exacting standards of real-world regulatory practice.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to work at the frontier of biomedical AI without leaving their area of expertise.
* Organization: Alignerr
* Type: Hourly Contract
* Location: Remote
* Commitment: 10–40 hours/week
What You'll Do
* Design and review clinical trial protocols used to generate high-quality, regulator-ready AI training datasets
* 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 agency expectations
* Provide expert feedback that shapes how AI models reason about clinical trial data, endpoints, and outcomes
* Help establish quality standards for how clinical evidence is represented and evaluated within AI systems
Who You Are
* Senior-level clinical scientist with hands‑on experience designing clinical trial protocols for regulatory submission
* Deep expertise interpreting clinical data for regulatory agencies (FDA, EMA, or equivalent)
* Strong grounding in clinical research methodology, biostatistics, or translational science
* Rigorous, detail‑oriented thinker who can identify gaps between AI‑generated outputs and real‑world regulatory standards
* Comfortable working independently and asynchronously in a remote environment
Nice to Have
* Prior experience with data annotation, data quality evaluation, or AI training workflows
* Background in pharmacovigilance, medical affairs, or clinical data management
* Familiarity with ICH guidelines, GCP, or similar regulatory frameworks
* Experience reviewing or contributing to regulatory dossiers or clinical study reports
Why Join Us
* Work directly on frontier AI systems shaping the future of clinical and biomedical research
* Fully remote and flexible — structure your hours around your existing commitments
* Freelance autonomy with the substance of high‑impact, intellectually demanding work
* Influence how AI understands, evaluates, and reasons about real‑world clinical evidence
* Collaborate with leading AI research teams and labs at the cutting edge of the field
* Potential for ongoing work and contract extension as new projects launch
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