Principal Clinical Scientist
Alignerr · Cambridge, England
CONTRACT
Posted Sep 7, 2026
Job Description
Principal Clinical Scientist (AI Training)
About The Role
What if your career designing and interpreting regulatory-grade clinical trials could directly shape how AI reasons about clinical evidence — at a global scale?
We're looking for a Principal Clinical Scientist to bring senior-level expertise into cutting-edge AI research workflows. You'll work alongside the world's leading AI labs, helping ensure the clinical data that trains and evaluates advanced AI systems meets the rigor, structure, and regulatory standards expected in real-world submissions.
This is a fully remote, flexible contract role built for senior clinical professionals who want to do meaningful, high-impact work on their own terms.
- 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 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 structured, expert feedback that directly improves how AI models reason about clinical trial data and real-world outcomes
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Senior-level clinical professional with hands-on experience designing clinical trial protocols for regulatory submission
- Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies
- Strong foundation in clinical research methodology, biostatistics, translational science, or a related discipline
- Naturally detail-oriented with high standards for scientific accuracy and data integrity
- Comfortable working independently and delivering structured, high-quality feedback
Nice to Have
- Prior experience with data annotation, data quality evaluation, or AI evaluation workflows
- Background in reviewing or auditing datasets for regulatory or scientific compliance
- Familiarity with AI tools or biomedical research platforms as an end user
Why Join Us
- Work directly on frontier AI systems impacting clinical and biomedical research worldwide
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the structure of meaningful, expert-level task-based work
- Influence how AI understands, evaluates, and communicates real-world clinical evidence
- Collaborate with leading AI research teams on genuinely novel scientific problems
- Potential for ongoing work and contract extension as new projects launch
About The Role
What if your career designing and interpreting regulatory-grade clinical trials could directly shape how AI reasons about clinical evidence — at a global scale?
We're looking for a Principal Clinical Scientist to bring senior-level expertise into cutting-edge AI research workflows. You'll work alongside the world's leading AI labs, helping ensure the clinical data that trains and evaluates advanced AI systems meets the rigor, structure, and regulatory standards expected in real-world submissions.
This is a fully remote, flexible contract role built for senior clinical professionals who want to do meaningful, high-impact work on their own terms.
- 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 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 structured, expert feedback that directly improves how AI models reason about clinical trial data and real-world outcomes
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Senior-level clinical professional with hands-on experience designing clinical trial protocols for regulatory submission
- Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies
- Strong foundation in clinical research methodology, biostatistics, translational science, or a related discipline
- Naturally detail-oriented with high standards for scientific accuracy and data integrity
- Comfortable working independently and delivering structured, high-quality feedback
Nice to Have
- Prior experience with data annotation, data quality evaluation, or AI evaluation workflows
- Background in reviewing or auditing datasets for regulatory or scientific compliance
- Familiarity with AI tools or biomedical research platforms as an end user
Why Join Us
- Work directly on frontier AI systems impacting clinical and biomedical research worldwide
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the structure of meaningful, expert-level task-based work
- Influence how AI understands, evaluates, and communicates real-world clinical evidence
- Collaborate with leading AI research teams on genuinely novel scientific problems
- Potential for ongoing work and contract extension as new projects launch
Additional Details
- City
- Cambridge
- State
- England
- Country
- GB
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