About the Role
What if your expertise in clinical trial design and regulatory science could directly shape how AI understands and evaluates real-world medical evidence?
We're partnering with the world's leading AI research labs to build and train advanced AI models — and we need senior clinical scientists to ensure the clinical knowledge powering these systems meets the highest standards of scientific rigor and regulatory integrity.
This is a fully remote, flexible contract role. No AI background required — just deep clinical expertise and a commitment to scientific quality.
- 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 datasets for AI training
- 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 standards
- Provide expert, structured feedback that directly improves how AI models reason about clinical data, trial outcomes, and biomedical evidence
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Senior-level clinical scientist with hands-on experience designing trial protocols for regulatory submission
- Deep expertise interpreting clinical data for major regulatory agencies (FDA, EMA, or equivalent)
- Strong background in clinical research methodology, biostatistics, or translational science
- Naturally rigorous and detail-oriented — you hold clinical data to the highest standards
- Clear and precise written communicator, comfortable providing structured, actionable feedback
Nice to Have
- Prior experience with data annotation, data quality frameworks, or evaluation systems
- Familiarity with AI tools or machine learning workflows in a clinical or biomedical context
- Background in drug development, medical devices, or health technology assessment
- Experience working across multiple therapeutic areas or global regulatory environments
Why Join Us
- Work directly on frontier AI systems that are transforming clinical and biomedical research
- Influence how AI understands, evaluates, and reasons about real-world clinical evidence
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the structure of meaningful, expert-level work
- Collaborate with leading AI research teams and scientists from around the world
- Potential for ongoing work and contract extension as new projects launch