Principal Clinical Scientist AI Training - Remote Contract

Further Details

Seeking a Principal Clinical Scientist for AI Training, a remote contract position focused on enhancing AI's understanding of biomedical data. This role requires deep expertise in clinical trial design and regulatory science to ensure AI models meet FDA, EMA, and equivalent agency standards. The opportunity involves designing protocols for AI training datasets, interpreting clinical trial outcomes, and providing expert feedback to refine AI's comprehension of clinical evidence. This is a flexible, hourly contract role for seasoned clinical scientists. You will work asynchronously, applying your critical evaluation skills to AI-generated analyses and identifying areas for improvement in AI's reasoning about clinical methodology. Contribute to frontier AI systems and reshape biomedical research from a remote, flexible setting.

Principal Clinical Scientist (AI Training) - Remote Contract Opportunity

This exciting contract role seeks a seasoned Principal Clinical Scientist to contribute to the advancement of AI in biomedical research. Working remotely, you will leverage your extensive background in clinical trial design and regulatory science to shape how sophisticated AI systems interpret complex medical data. This position is ideal for professionals who want to make a significant impact on frontier AI technologies while maintaining a flexible work schedule. Key responsibilities include designing and scrutinizing clinical trial protocols for AI training datasets, ensuring regulatory compliance and accuracy. You will also evaluate AI-generated clinical analyses, providing critical feedback to enhance AI's understanding of clinical evidence and methodology. Successful candidates will benefit from these professional growth. This role offers a unique chance to influence the development of AI in healthcare.

• Job Title: Principal Clinical Scientist (AI Training)
• Location: Remote (Castilla y León, Spain)
• Employment Type: Hourly Contract
• Commitment: 10–40 hours/week
• Key Skills: Clinical trial protocol design, regulatory science expertise, data interpretation, critical evaluation of scientific outputs, strong communication.
• Qualifications: Senior-level clinical scientist with deep expertise in clinical research methodology, biostatistics, or translational science.
• Company: Alignerr
• Posted: 03 November, 2026
• Closing Date: 18 December, 2026

Skills

• Senior-level clinical scientist with hands-on experience designing and reviewing clinical trial protocols for regulatory submission
• Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent
• Strong command of clinical research methodology, biostatistics, or translational science
• Able to critically evaluate complex scientific outputs and communicate findings with precision
• Detail-oriented and systematic — you hold work to a high standard

Duties and Responsibilities:

• Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets for AI training and evaluation
• Interpret and audit clinical trial results, ensuring accuracy, consistency, and regulatory relevance
• Evaluate AI-generated clinical analyses for scientific soundness and alignment with regulatory expectations
• Identify gaps, errors, and weaknesses in how AI models reason about clinical outcomes and trial methodology
• Provide structured expert feedback that directly improves how frontier AI systems understand real-world clinical evidence
• Work independently and asynchronously — fully on your own schedule

How to apply

💼 Interested candidates are invited to apply for this unique remote contract opportunity. 👉 To submit your application, please visit the official application link provided. 📝 Ensure your application includes a comprehensive CV detailing your experience in clinical trial design, regulatory science, and data interpretation. ⏳ The deadline for applications is December 18, 2026. Early submissions are encouraged. Additionally, career development are available for qualified candidates. ✅ Applicants should possess senior-level expertise in clinical research methodology, biostatistics, or translational science. 🌐 For further details and to initiate the application process, please use the provided link.