At a Glance
- Tasks: Design clinical trial protocols and evaluate AI-generated analyses for regulatory compliance.
- Company: Alignerr, a leader in AI research with a focus on clinical evidence.
- Benefits: Fully remote, flexible hours, and the chance to work on impactful AI projects.
- Other info: Collaborate with top AI teams and enjoy freelance autonomy with meaningful projects.
- Why this job: Shape the future of AI in clinical research and make a real-world impact.
- Qualifications: Senior clinical scientist with experience in regulatory submissions and clinical data interpretation.
The predicted salary is between 10 - 40 $ per hour.
What if your deep expertise in clinical trial design and regulatory science could directly shape how AI understands and reasons about clinical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to cutting-edge AI research workflows. You'll work alongside world-leading AI labs to ensure that clinical data used to train and evaluate advanced AI systems meets the exacting standards expected in real-world regulatory submissions — FDA, EMA, and beyond.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to apply their expertise in a high-impact, forward-looking environment.
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 expert, structured feedback that directly improves how AI models reason about clinical trial data, outcomes, and evidence
- Help establish the quality bar for clinical content used across frontier AI research projects
Who You Are
- Senior clinical scientist with hands-on 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 grounding in clinical research methodology, biostatistics, translational science, or a closely related discipline
- Naturally rigorous and detail-oriented — you hold clinical data to the highest standards
- Comfortable working independently and delivering structured, high-quality feedback in a remote environment
Nice to Have
- Prior experience with data annotation, data quality frameworks, or AI evaluation systems
- Background in pharmacology, oncology, rare disease, or other specialized therapeutic areas
- Familiarity with AI tools or content evaluation platforms
Why Join Us
- Work directly on frontier AI systems making a real impact on clinical and biomedical research
- Influence how AI understands, evaluates, and communicates real-world clinical evidence at scale
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the structure of meaningful, expert-level project work
- Collaborate with leading AI research teams on some of the most ambitious AI projects in existence
- Potential for ongoing work and contract extension as new projects launch
Principal Clinical Scientist in Newcastle employer: Alignerr
As a leading AI research partner, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a real difference in public health. With flexible hours and competitive pay, our Remote Health Policy & AI Content Specialist role offers unique opportunities for professional growth while contributing to meaningful projects that advance health equity. Join us to be part of a dynamic team dedicated to shaping the future of health information through cutting-edge AI technology.
