At a Glance
- Tasks: Design clinical trials and ensure AI systems meet regulatory standards.
- Company: Alignerr, a leader in AI development for clinical research.
- Benefits: Fully remote, flexible hours, and freelance autonomy.
- Other info: Collaborate with top AI researchers globally and influence real-world clinical evidence.
- Why this job: Shape the future of AI in healthcare while working on your own terms.
- Qualifications: Senior-level clinical scientist with regulatory submission experience.
The predicted salary is between 10 - 40 $ per hour.
Principal Clinical Scientist (AI Training)
About The Role
What if your expertise in clinical trial design and regulatory science could directly shape how AI reasons about medical evidence for researchers and clinicians worldwide?
We're looking for a Principal Clinical Scientist to bring senior-level clinical rigor to cutting-edge AI development.
You'll work with leading AI research teams to ensure that the clinical data powering next-generation AI systems meets the same standards expected in real-world regulatory submissions.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to do meaningful 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
- Interpret and audit clinical trial results to ensure accuracy, consistency, and regulatory relevance
- Evaluate AI-generated clinical analyses for scientific soundness and alignment with regulatory expectations
- Identify gaps in how AI models reason about clinical outcomes and provide expert corrective feedback
- Help establish quality standards for clinical data used across AI research workflows
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Senior-level clinical scientist with hands-on experience designing protocols for regulatory submission
- Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies
- Strong grounding in clinical research methodology, biostatistics, or translational science
- Naturally rigorous — you hold clinical data to the highest standards of accuracy and consistency
- Clear communicator who can translate complex clinical concepts into structured, actionable feedback
- Nice to Have
- Prior experience with data annotation, data quality review, or AI evaluation workflows
- Background in pharmacovigilance, medical affairs, or clinical operations
- Familiarity with AI tools or machine learning systems in a biomedical context
- Experience contributing to cross-functional or distributed research teams
- Why Join Us
- Work directly on frontier AI systems shaping the future of 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 communicates real-world clinical evidence
- Collaborate with leading AI research labs and scientists from around the world
- Potential for ongoing work and contract extension as new projects launch
- #J-18808-Ljbffr
Principal Clinical Scientist in Adelaide 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.
