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 labs and enjoy freelance autonomy in your work.
- 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.
About The Role
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.
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 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 Sydney 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.
