Business Services & Consulting • all cities, SC 41
Principal Clinical Scientist (41)
all cities, SC 41On-sitePosted 2 hours ago
Business Services & Consulting
About the Role
Principal Clinical Scientist
What if your career designing rigorous clinical trials and interpreting regulatory-grade data could directly shape how AI understands biomedical science? We're looking for a Principal Clinical Scientist to bring senior-level clinical expertise into the development of cutting-edge AI systems — ensuring these models reason about clinical evidence the way the world's top regulatory scientists do.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to do meaningful work at the frontier of AI and biomedical research.
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 alignment with regulatory standards
Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance
Provide expert, structured feedback that shapes how AI models reason about clinical trial data, outcomes, and evidence
Work independently and asynchronously — fully on your own schedule
Who You Are
Senior-level experience designing clinical trial protocols intended for regulatory submission
Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent bodies
Strong command of clinical research methodology, biostatistics, or translational science
Rigorous, detail-oriented thinker who can translate complex clinical concepts into clear, structured feedback
Self-motivated and reliable when working independently without supervision
Nice to Have
Prior experience with data annotation, data quality review, or AI evaluation workflows
Background in regulatory affairs, medical writing, or clinical operations
Familiarity with AI tools or machine learning applications in healthcare or life sciences
Experience contributing to multi-site or global clinical trials
Why Join Us
Work directly on frontier AI systems making an impact in clinical and biomedical research
Fully remote and flexible — work when and where it suits you
Freelance autonomy with the structure of meaningful, expert-level work
Influence how AI understands, evaluates, and reasons about real-world clinical evidence
Collaborate with world-leading AI research teams and labs
Potential for ongoing work and contract extension as new projects launch
Principal Clinical Scientist
What if your career designing rigorous clinical trials and interpreting regulatory-grade data could directly shape how AI understands biomedical science? We're looking for a Principal Clinical Scientist to bring senior-level clinical expertise into the development of cutting-edge AI systems — ensuring these models reason about clinical evidence the way the world's top regulatory scientists do.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to do meaningful work at the frontier of AI and biomedical research.
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 alignment with regulatory standards
Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance
Provide expert, structured feedback that shapes how AI models reason about clinical trial data, outcomes, and evidence
Work independently and asynchronously — fully on your own schedule
Who You Are
Senior-level experience designing clinical trial protocols intended for regulatory submission
Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent bodies
Strong command of clinical research methodology, biostatistics, or translational science
Rigorous, detail-oriented thinker who can translate complex clinical concepts into clear, structured feedback
Self-motivated and reliable when working independently without supervision
Nice to Have
Prior experience with data annotation, data quality review, or AI evaluation workflows
Background in regulatory affairs, medical writing, or clinical operations
Familiarity with AI tools or machine learning applications in healthcare or life sciences
Experience contributing to multi-site or global clinical trials
Why Join Us
Work directly on frontier AI systems making an impact in clinical and biomedical research
Fully remote and flexible — work when and where it suits you
Freelance autonomy with the structure of meaningful, expert-level work
Influence how AI understands, evaluates, and reasons about real-world clinical evidence
Collaborate with world-leading AI research teams and labs
Potential for ongoing work and contract extension as new projects launch
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 alignment with regulatory standards
Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance
Provide expert, structured feedback that shapes how AI models reason about clinical trial data, outcomes, and evidence
Work independently and asynchronously — fully on your own schedule
Senior-level experience designing clinical trial protocols intended for regulatory submission
