Principal Clinical Scientist

Alignerr Corp.; Tampa (FL); Remote; USD 96,000 - 179,000; Part time

Job summary

Alignerr Corp. seeks a Principal Clinical Scientist (AI Training) for a remote, hourly contract. You will design and review clinical trial data used to train regulator-ready AI systems, ensuring FDA/EMA standards are met.

You will audit AI-generated analyses, provide structured feedback, and work asynchronously on a flexible schedule (10–40 hours/week) with potential extension. Senior-level expertise in regulatory submissions, biostatistics, and translational science is required, with a track

Qualifications

• Senior clinical scientist with regulatory submission experience.
• Experience designing protocols for regulatory use.
• Ability to interpret regulatory guidelines and translate into AI training data.

Responsibilities

• Design and review clinical trial protocols used to generate regulator-ready AI training datasets
• Interpret and audit clinical trial results for accuracy, consistency, and regulatory relevance
• Evaluate AI-generated clinical analyses for scientific soundness and regulatory alignment
• Provide expert, structured feedback to improve AI model reasoning on clinical data
• Work independently and asynchronously on a flexible schedule

Skills

Regulatory submissions

Clinical trial design

Biostatistics

Regulatory knowledge

Independent work

Education

MD/PhD in life sciences

Tools

Statistical software

Regulatory databases

Job description

Principal Clinical Scientist (AI Training)

About The Role

What if your career-long expertise in clinical trial design and regulatory science could directly influence how AI understands medicine? We're looking for a Principal Clinical Scientist to bring senior-level rigor to AI-driven research workflows — helping ensure that the clinical knowledge embedded in next-generation AI systems meets the standards expected in real-world regulatory submissions.

This is a fully remote, flexible contract role designed 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 AI training datasets
• Interpret and audit clinical trial results for accuracy, consistency, and regulatory relevance
• Evaluate AI-generated clinical analyses for scientific soundness and alignment with regulatory expectations
• Provide expert, structured feedback that improves how AI models reason about clinical trial data and real-world outcomes
• Work independently and asynchronously — entirely 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 bodies
• Strong grounding in clinical research methodology, biostatistics, or translational science
• Rigorous, detail-oriented thinker who can translate complex clinical nuance into clear, structured feedback
• Comfortable working independently in a remote, task-based environment

Nice to Have

• Prior experience with data annotation, data quality assurance, or AI evaluation systems
• Familiarity with AI-generated content or machine learning workflows in a clinical or research context
• Background spanning multiple therapeutic areas or regulatory jurisdictions

Why Join Us

• Work directly on frontier AI systems that are reshaping clinical and biomedical research
• Influence how AI understands, evaluates, and reasons about real-world clinical evidence
• Fully remote and flexible — work when and where it suits you
• Freelance autonomy with the structure of meaningful, high-impact, task-based work
• Collaborate with leading AI research teams on genuinely novel problems
• Potential for ongoing work and contract extension as new projects launch