Alignerr logo

Principal Clinical Scientist

Alignerr
Department:Accounting
Type:REMOTE
Region:Adelaide
Location:Adelaide, South Australia, Australia
Experience:Mid-Senior level
Estimated Salary:A$83,200 - A$166,400
Skills:
CLINICAL TRIAL DESIGNREGULATORY SUBMISSIONFDAEMACLINICAL RESEARCH METHODOLOGYBIOSTATISTICSTRANSLATIONAL SCIENCEDATA ANNOTATIONDATA QUALITYEVALUATION SYSTEMS
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Job Description

Posted on: February 14, 2026

About The Job At Alignerr, we partner with the world’s leading AI research teams and labs to build and train cutting-edge AI models. We are seeking a Principal Clinical Scientist to bring senior-level expertise in clinical trial design and regulatory-grade data interpretation into AI-driven research workflows. In this role, you will help ensure that clinical data used to train and evaluate advanced AI systems meets the rigor, structure, and regulatory standards expected in real-world submissions. Organization: Alignerr Position: Principal Clinical Scientist Type: Hourly Contract Compensation: $40–$80 /hour 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.
  • 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.
  • Provide expert feedback to improve how AI models reason about clinical trial data and outcomes.

What We’re Looking For

  • Senior-level experience designing clinical trial protocols for regulatory submission.
  • Deep expertise interpreting clinical data for agencies such as FDA, EMA, or equivalent.
  • Strong background in clinical research methodology, biostatistics, or translational science.

Preferred

  • Prior experience with data annotation, data quality, or evaluation systems

Why Join Us

  • Competitive pay and flexible remote work.
  • Work directly on frontier AI systems impacting clinical and biomedical research.
  • Influence how AI understands and evaluates real-world clinical evidence.
  • Freelance perks: autonomy, flexibility, and global collaboration.
  • Potential for contract extension.

Application Process (Takes 15–20 min)

  • Submit your resume
  • Complete a short screening
  • Project matching and onboarding

PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Originally posted on LinkedIn

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