Principal Clinical Scientist

Alignerr Corp.; Remote; GBP 150,000 - 200,000; Part time

Job summary

A leading AI research firm is seeking a Principal Clinical Scientist with senior-level expertise in clinical trial design and data interpretation. In this remote role, you'll ensure that clinical data meets regulatory standards for AI systems. Responsibilities include designing trial protocols, auditing results, and providing feedback to enhance AI analytics. Competitive pay and flexible work are offered, with potential for contract extensions. Apply now to influence cutting-edge AI in biomedical research.

Benefits

Competitive pay

Flexible remote work

Freelance autonomy and collaboration

Qualifications

• Experience in regulatory-grade data interpretation.
• Familiarity with FDA, EMA, or equivalent agencies.
• Expertise in biostatistics or translational science.

Responsibilities

• Design and review clinical trial protocols.
• Interpret and audit clinical trial results.
• Evaluate AI-generated clinical analyses.
• Provide feedback to improve AI models.

Skills

Senior-level experience designing clinical trial protocols

Deep expertise interpreting clinical data

Strong background in clinical research methodology

Job description

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.