Principal Clinical Scientist - AI Training & Regulatory Science (Remote)

Further Details

Seeking a Principal Clinical Scientist to drive AI innovation in biomedical research through expert input on clinical trial design and regulatory science. This remote contract position allows experienced professionals to influence how AI systems process complex clinical data, aligning with FDA and EMA standards. Your role will involve designing protocols, interpreting results, and evaluating AI outputs to ensure scientific accuracy and regulatory compliance. This position represents excellent vacancies in the region. This opportunity is perfect for individuals with a strong background in clinical research methodology, biostatistics, or translational science. You will critically assess scientific findings and provide precise feedback to improve AI's comprehension of clinical outcomes and trial methodologies. Join a leading AI research team and contribute to the advancement of AI in healthcare from anywhere in the world.

Principal Clinical Scientist - AI Training & Regulatory Science

Embark on a groundbreaking career as a Principal Clinical Scientist, playing a pivotal role in advancing AI development within the biomedical sector. This fully remote, flexible contract position offers an exceptional platform to apply your extensive knowledge of clinical trial design and regulatory science. You will be instrumental in shaping sophisticated AI systems, ensuring they process complex clinical data with the precision and adherence to standards expected by global authorities like the FDA and EMA. This is a unique chance to contribute to transformative healthcare innovations while maintaining a flexible work-life balance.

This role is designed for experienced clinical scientists who are passionate about contributing to novel AI applications. Your responsibilities will encompass the meticulous design and review of clinical trial protocols, crucial for generating high-quality, regulator-ready datasets essential for AI training and evaluation. You will also be tasked with interpreting and auditing clinical trial outcomes, verifying their accuracy, consistency, and regulatory alignment. Furthermore, you will critically assess AI-generated clinical analyses, ensuring their scientific validity and compliance with regulatory benchmarks. By identifying and addressing any shortcomings in AI models' reasoning regarding clinical outcomes and trial methodologies, you will provide invaluable expert feedback that directly enhances AI's understanding of real-world clinical evidence.

• Job Title: Principal Clinical Scientist (AI Training)
• Location: Canarias, Spain (Remote)
• Company: Alignerr
• Contract Type: Hourly Contract (10-40 hours/week)
• Key Responsibilities: AI model evaluation, clinical protocol design, regulatory compliance
• Required Expertise: Clinical trial design, regulatory science, biostatistics, data interpretation
• Opportunity: Shape frontier AI systems in biomedical research

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 with a high standard for 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

Interested candidates are invited to submit their applications through the official Eurojobs portal. Please ensure all required documentation is prepared and submitted by the closing date to be considered for this exciting opportunity.

• Step 1: Visit the Eurojobs website and navigate to the job listing for the Principal Clinical Scientist position.
• Step 2: Click on the 'Apply Now' button to initiate the application process.
• Step 3: Complete the online application form with accurate and up-to-date personal and professional information.
• Step 4: Upload your Curriculum Vitae (CV) detailing your relevant experience in clinical trial design, regulatory science, and AI training.
• Step 5: Ensure your CV highlights your expertise in interpreting clinical data for regulatory agencies and your command of clinical research methodology.
• Step 6: Review all submitted information for accuracy before final submission.
• Application Deadline: 18 December 2026
• Job Reference: 6402276095864864768324626
• Platform: Eurojobs