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Freelance Biomedical Device Jobs (NOW HIRING)

Experience reviewing or contributing to clinical evidence packages for drug, device, or diagnostic ... biomedical research * Fully remote and flexible - work when and where it suits you * Freelance ...

Associate Scientific Director About Us Virgo Health works for pharmaceutical, biotech, and device ... Brief freelancers as necessary Work with editorial assistant (or account executive) to manage ...

Associate Scientific Director About Us Virgo Health works for pharmaceutical, biotech, and device ... freelancers as necessary • Work with editorial assistant (or account executive) to manage ...

Freelance Biomedical Device information

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How much do freelance biomedical device jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for freelance biomedical device in the United States is $62.54, according to ZipRecruiter salary data. Most workers in this role earn between $60.34 and $68.27 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Biomedical Device jobs? The most popular types of Biomedical Device jobs are:

Principal Clinical Scientist

Alignerr

Indianapolis, IN • Remote

Full-time

Posted 11 days ago


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 shape how AI understands and reasons about medical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to frontier AI research - ensuring the clinical data and analyses powering next-generation AI systems meet the same exacting standards expected in real-world regulatory submissions.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to contribute to something genuinely new. No AI background required - just deep command of clinical research and a sharp eye for scientific quality.
  • Organization
    : Alignerr
  • Type
    : Hourly Contract
  • Location
    : Remote
  • Commitment
    : 10-40 hours/week
  • What You'll Do
    • Design and critically review clinical trial protocols used to generate high-quality, regulatory-grade datasets for AI training
    • Interpret and audit clinical trial results for accuracy, consistency, and alignment with regulatory expectations
    • Evaluate AI-generated clinical analyses for scientific soundness and methodological integrity
    • Provide structured expert feedback that directly improves how AI models reason about clinical evidence, outcomes, and trial data
    • 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 global bodies
    • Strong grounding in clinical research methodology, biostatistics, or translational science
    • Naturally detail-oriented with a rigorous, systematic approach to evaluating scientific quality
    • Clear and precise written communicator - able to document findings and feedback with authority
    • No prior AI or tech experience required
    Nice to Have
    • Prior involvement in data annotation, data quality assurance, or evaluation systems
    • Experience reviewing or contributing to clinical evidence packages for drug, device, or diagnostic submissions
    • Background spanning multiple therapeutic areas or trial phases
    • Familiarity with AI-generated content or model evaluation workflows
    Why Join Us
    • Work directly on frontier AI systems with real impact on 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
    • Potential for ongoing work and contract extension as new projects launch