Principal Clinical Scientist

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

Job summary

A leading AI research firm seeks a Principal Clinical Scientist to ensure the clinical data used for AI systems meets regulatory standards. Responsibilities include designing trial protocols, interpreting data from regulatory agencies, and enhancing AI's ability to analyze clinical evidence. This remote role offers competitive pay, flexible hours, and the chance to influence AI in drug development. Candidates should have senior-level experience and a strong background in clinical research methodologies.

Benefits

Competitive pay

Flexible remote work

Autonomy and flexibility

Global collaboration

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.

Responsibilities

• Design and review clinical trial protocols used to generate high-quality datasets.
• Interpret and audit clinical trial results for accuracy and regulatory relevance.
• Evaluate AI-generated clinical analyses for soundness and regulatory alignment.
• Provide expert feedback to enhance AI models' reasoning about clinical data.

Skills

Designing clinical trial protocols

Interpreting clinical data

Clinical research methodology

Biostatistics

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.