Principal Clinical Scientist
Posted Today by Alignerr
Negotiable
Undetermined
Remote
London, England, United Kingdom
Summary: The Principal Clinical Scientist at Alignerr will leverage senior-level expertise in clinical trial design and regulatory data interpretation to enhance AI-driven research workflows. This role involves ensuring that clinical data meets regulatory standards for AI model training and evaluation. The position is remote and offers flexible hours, focusing on high-quality, regulator-ready datasets. The ideal candidate will have extensive experience in clinical research and a strong understanding of regulatory expectations.
Key Responsibilities:
- 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.
Key Skills:
- 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.
- Prior experience with data annotation, data quality, or evaluation systems preferred.
Salary (Rate): £80.00/hour
City: London
Country: United Kingdom
Working Arrangements: remote
IR35 Status: undetermined
Seniority Level: Senior
Industry: IT
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.