Principal Clinical Scientist - AI Training (Remote, Spain)

Further Details

Seeking a Principal Clinical Scientist with extensive experience in clinical trial design and regulatory science to enhance AI-driven research workflows. This role focuses on ensuring AI models accurately interpret clinical data, aligning with FDA, EMA, and global agency standards. It's a fully remote, flexible contract position for seasoned clinical scientists. Your responsibilities will include designing and reviewing protocols for AI training datasets, interpreting trial results for regulatory relevance, and evaluating AI analyses. You will provide expert feedback to improve AI systems' understanding of real-world clinical evidence, working independently on your own schedule.

Principal Clinical Scientist - AI Training Opportunities in Spain

Discover a groundbreaking career path as a Principal Clinical Scientist focused on AI training within the vibrant region of Andalucía, Spain. This unique, fully remote contract position invites seasoned professionals to leverage their deep expertise in clinical trial design and regulatory science. Successful candidates will benefit from these job openings. You will be instrumental in shaping the future of artificial intelligence in biomedical research by ensuring AI models accurately interpret complex clinical data, adhering strictly to global regulatory benchmarks set by agencies like the FDA and EMA. This role offers unparalleled flexibility, allowing you to work on your own schedule while contributing to truly innovative projects. It's an exceptional chance to influence how AI understands, evaluates, and communicates real-world clinical evidence at scale, collaborating with leading AI research teams. If you possess a meticulous approach and a passion for advancing scientific understanding through technology, this opportunity is for you.

• Job Title: Principal Clinical Scientist (AI Training)
• Location: Andalucía, Spain (Fully Remote)
• Employment Type: Hourly Contract
• Commitment: 10–40 hours per week
• Key Responsibilities: Designing and reviewing clinical trial protocols, interpreting clinical data, evaluating AI analyses, and providing expert feedback.
• Required Qualifications: Senior-level clinical scientist with regulatory submission experience, strong understanding of clinical research methodology, and excellent analytical skills.
• Desired Skills: Familiarity with AI tools, machine learning workflows, pharmacology, epidemiology, or regulatory affairs.

Skills

• Senior-level clinical scientist expertise
• Hands-on experience designing clinical trial protocols
• Experience reviewing clinical trial protocols for regulatory submission
• Deep expertise interpreting clinical data for regulatory agencies (FDA, EMA, etc.)
• Strong command of clinical research methodology
• Proficiency in biostatistics or translational science
• Ability to critically evaluate complex scientific outputs
• Precision in communicating findings
• Detail-oriented and systematic approach
• High standards for work quality

Duties and Responsibilities:

• Design and review clinical trial protocols for AI training datasets
• Generate high-quality, regulator-ready datasets for AI training and evaluation
• Interpret clinical trial results
• Audit clinical trial results for accuracy, consistency, and regulatory relevance
• Evaluate AI-generated clinical analyses for scientific soundness
• Ensure AI analyses align with regulatory expectations
• Identify gaps, errors, and weaknesses in AI model reasoning
• Provide structured expert feedback to improve AI systems
• Work independently and asynchronously on a flexible schedule

How to apply

Embark on this exciting career opportunity by following these steps to submit your application:

• Step 1: Access the Application Portal 💼 Visit the official Eurojobs application link provided to initiate your application process.
• Step 2: Review Job Details 🔎 Carefully read through the complete job description, responsibilities, and required qualifications to ensure a strong match with your profile.
• Step 3: Prepare Your Application Documents 📝 Gather your most up-to-date Curriculum Vitae (CV) detailing your relevant experience in clinical trial design and regulatory science. Ensure it highlights your expertise in interpreting clinical data for regulatory bodies.
• Step 4: Submit Your Application 👉 Click on the 'Apply Now' button on the Eurojobs page to formally submit your application.
• Step 5: Await Confirmation ⏳ You will receive confirmation once your application has been successfully submitted.
• Important Note: This is a freelance/contract position with flexible working hours. Ensure your CV clearly outlines your availability and experience with independent work.