Principal Clinical Scientist - AI Training (Remote)

Further Details

This Principal Clinical Scientist position focuses on AI training within the biomedical field, offering a remote, flexible contract. The role demands senior-level expertise in clinical trial design and regulatory science to refine AI models' understanding of clinical data. Successful candidates will ensure AI outputs align with FDA, EMA, and other global regulatory expectations, contributing to the development of advanced AI systems for research. The core responsibilities involve designing and reviewing protocols for high-quality, regulator-ready datasets used in AI training and evaluation. You will interpret and audit clinical trial results for accuracy and regulatory compliance, critically assessing AI-generated analyses. This role is perfect for experienced clinical scientists passionate about shaping the future of AI in healthcare and research.

Principal Clinical Scientist - AI Training Opportunities in Spain

Alignerr is actively seeking a highly experienced Principal Clinical Scientist to contribute to cutting-edge AI development in the biomedical sector. This is a unique opportunity for professionals with a strong background in clinical trial design and regulatory science to influence the evolution of AI in healthcare. The role is fully remote, offering flexibility and autonomy to work on impactful projects shaping how AI understands complex clinical data.

As a Principal Clinical Scientist, you will be instrumental in ensuring AI models adhere to the rigorous standards expected by global regulatory bodies like the FDA and EMA. Your expertise will guide the interpretation and evaluation of clinical data, enhancing the accuracy and reliability of AI-driven research workflows. This position is ideal for those passionate about bridging clinical science and artificial intelligence.

• Job Title: Principal Clinical Scientist (AI Training)
• Location: Euskadi, Spain (Fully Remote)
• Company: Alignerr
• Contract Type: Hourly Contract (10-40 hours/week)
• Key Responsibilities: Designing clinical trial protocols, evaluating AI analyses, providing expert feedback.
• Required Qualifications: Senior-level clinical scientist with regulatory submission experience, strong data interpretation skills.

This position represents excellent latest recruitment in the region.

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 approach to work

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 on your own schedule

How to apply

• Explore the Opportunity: Visit the Eurojobs website and navigate to the job listing for the Principal Clinical Scientist (AI Training) position.
• Review Details: Carefully read the full job description, responsibilities, and required qualifications to ensure a strong match with your professional background.
• Initiate Application: Click on the 'Apply Now' button prominently displayed on the job advertisement page.
• Complete Application Form: You will be directed to the application portal where you need to fill out the required fields accurately.
• Submit Supporting Documents: Upload your updated Curriculum Vitae (CV) and any other relevant supporting documents as requested by the employer.
• Confirmation: Await confirmation of your application submission.
• Contact Information: For further inquiries, please refer to the contact details provided on the Eurojobs platform or the company's official channels if available.
• Deadline: Ensure your application is submitted before the closing date of 18 December 2026.