Principal Clinical Scientist
Behavioral Health Market Context
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Job Description
ed 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.
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.
Qualifications
- •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
- •Influence how AI understands and evaluates real-world clinical evidence
- •Project matching and onboarding
Benefits
- •: $40-$80 /hour
- •Competitive pay and flexible remote work
- •Work directly on frontier AI systems impacting clinical and biomedical research
- •Freelance perks: autonomy, flexibility, and global collaboration
- •Potential for contract extension
Responsibilities
- •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
- •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
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