Principal Clinical Scientist

Alignerr Corp.; Remote; GBP 125,000 - 150,000; Part time

Job summary

A leading AI research company is seeking a Principal Clinical Scientist to leverage senior-level expertise in clinical trial design and data interpretation. This remote role involves ensuring that clinical data meets rigorous standards for AI-driven research. The ideal candidate will possess deep expertise for regulatory submissions and a strong background in clinical research. The position offers competitive pay, flexible work hours, and potential for contract extension in an innovative environment.

Benefits

Competitive pay

Flexible remote work

Freelance autonomy and flexibility

Qualifications

• Deep expertise interpreting clinical data for regulatory bodies like FDA or EMA.
• Experience designing clinical trial protocols for regulatory submission is essential.
• Prior experience with data annotation or evaluation systems is preferred.

Responsibilities

• Design and review clinical trial protocols for high-quality datasets.
• Interpret clinical trial results ensuring regulatory relevance.
• Evaluate AI-generated analyses for scientific soundness.

Skills

Senior-level experience in clinical trial design

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.