Alignerr
Principal Clinical Scientist
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Principal Clinical Scientist (AI Training)
About the Role
What if your decades 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 one of the most consequential frontiers in technology — AI systems that interpret and generate clinical data.
This is a fully remote, flexible contract role for experienced clinical scientists who want to make an outsized impact without the constraints of a traditional position. You'll work alongside leading AI research labs to ensure frontier models handle clinical evidence the way regulators — and patients — deserve.
Organization: Alignerr Type: Hourly Contract Location: Remote Commitment: 10–40 hours/week
What You'll Do
- Design and critically review clinical trial protocols used to generate high-quality, regulator-ready training datasets for AI systems
- Interpret and audit clinical trial results to ensure accuracy, consistency, and alignment with regulatory standards (FDA, EMA, or equivalents)
- Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance, spotting errors that only a seasoned expert would catch
- Provide structured, expert feedback that directly shapes how AI models reason about:
- Clinical trial design
- Data
- Outcomes
- Help establish the gold standard for how AI understands and communicates clinical evidence
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Who You Are
You’re a senior-level clinical scientist with:
- Hands-on experience designing clinical trial protocols for regulatory submission
- Deep expertise in interpreting clinical data for regulatory agencies such as:
- FDA
- EMA
- Equivalent bodies
- Strong grounding in:
- Clinical research methodology
- Biostatistics
- Translational science
- An innate details-first mindset who holds clinical evidence to the highest standard
- Comfort in an asynchronous, remote work environment
Get help with your application
Your very own career expert that helps elevate your application to the next level.
Nice to Have
- Prior experience in:
- Data annotation
- Data quality frameworks
- Evaluation systems
- Background in:
- AI, digital health, or clinical decision support tools
- Experience across:
- Multiple therapeutic areas
- Various trial phases
- Familiarity with:
- ICH guidelines
- GCP standards
- Submission dossier preparation
Why Join Us
- Work directly on frontier AI systems that will shape the future of clinical and biomedical research
- Fully remote and flexible — structure your work around your life, not the other way around
- Freelance autonomy for high-stakes, meaningful work
- Influence how AI systems understand, evaluate, and communicate real-world clinical evidence at scale
- Collaborate with world-class AI research teams and labs on cutting-edge projects
- Potential for ongoing work and contract extension as new projects launch
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills