Senior AI Clinical Scientist - Remote Contract in Spain

Further Details

Alignerr Corp. is recruiting a Principal Clinical Scientist for an AI Training role, offering an hourly remote contract. The position requires designing and reviewing regulatory-ready clinical trial protocols for AI training and evaluation, ensuring scientific rigor and compliance. Key responsibilities include auditing trial results for regulatory relevance and evaluating AI-generated analyses for scientific soundness. The role demands identifying gaps in AI reasoning and methodology, all while working autonomously from a remote location. This is a significant opportunity for experienced clinical scientists to engage with cutting-edge AI technologies and contribute to regulatory advancements. The company values autonomous work and offers flexibility for professionals seeking a remote contract role. This position represents excellent latest recruitment in the region.

Senior Clinical Scientist - AI Training (Remote)

Alignerr Corp. is currently seeking a highly skilled Principal Clinical Scientist to join their team for an hourly remote contract. This role is pivotal in shaping the future of AI in clinical research by designing and scrutinizing regulatory-ready protocols for AI training and evaluation. You will play a crucial role in ensuring that AI-driven analyses meet stringent scientific and regulatory standards.

This exciting remote opportunity offers the chance to work autonomously and contribute significantly to the development and validation of AI methodologies within clinical trials. The ideal candidate will possess a deep understanding of clinical science, AI principles, and regulatory affairs, coupled with a proactive approach to problem-solving.

• Position: Principal Clinical Scientist, AI Training (Remote)
• Contract Type: Hourly Contract
• Location: Remote, Spain (Andalucía)
• Key Focus: Regulatory protocol design, AI evaluation, scientific soundness
• Required: Experience in clinical trial protocol development and AI analysis

Skills

• Design regulatory-ready clinical trial protocols
• Review clinical trial protocols for AI training and evaluation
• Audit trial results for regulatory relevance
• Evaluate AI-generated analyses for scientific soundness
• Identify gaps in AI reasoning and methodology
• Work autonomously

Duties and Responsibilities:

• Design and review regulatory-ready clinical trial protocols for AI training and evaluation
• Audit trial results for regulatory relevance
• Evaluate AI-generated analyses for scientific soundness and regulatory alignment
• Identify gaps in AI reasoning about outcomes and methodology
• Work remotely and autonomously

How to apply

• Prepare your application: Ensure your Curriculum Vitae (CV) is up-to-date and clearly highlights your experience in clinical science, AI training, and regulatory affairs.
• Visit the application portal: Navigate to the official application link provided for this vacancy.
• Submit your application: Complete the online application form accurately and attach all required documents, including your CV.
• Application Deadline: All applications must be submitted no later than 18 December 2026.
• Confirmation: Upon successful submission, you may receive a confirmation email.
• 👉 Visit the application link provided to submit your details.