Senior AI Clinical Product Researcher in London

Odin Vision is a multi-award-winning company that provides state-of-the-art AI-enabled software applications for endoscopic procedures. These applications aid clinicians in the detection and diagnosis of disease, supporting higher quality care, improved patient outcomes, and better value for healthcare payers.

We are looking for a full-time Senior AI Clinical Product Researcher to design and execute clinical research to support AI medical device product development, clinical performance validation, and regulatory evidence generation. The role applies deep clinical research expertise to generate high-quality, decision-ready evidence that informs product design, usability, and clinical claims.

This full-time hybrid role requires national and international travel (UK, EU, & US) and attendance at live endoscopy procedures.

Salary range: £50k-60K

Key Responsibilities:

• Clinical Research Execution: Design, execute, and analyse clinical research supporting AI-based medical devices, including real-world performance evaluations, usability/human factors engineering, literature reviews, pilot studies, and clinical investigations.
• Develop study protocols, analysis plans, and supporting documentation in line with approved methodologies and regulatory expectations.
• Conduct clinical data collection, analysis, and synthesis to generate clear, evidence-based insights.
• Monitor study progress to ensure adherence to protocols, timelines, and quality standards, and identify and elevate issues as appropriate.

• Evidence Generation & Documentation: Lead the preparation of research reports, literature reviews, and supporting documentation.
• Ensure research outputs are scientifically robust, fit for regulatory use, and directly applicable to product and design decision-making.
• Contribute content to clinical evaluation documentation and other regulatory-facing materials under guidance from senior leadership.

• Cross-Functional Collaboration: Collaborate with and coordinate activities across internal teams, including Clinical Research, Human Factors, AI Software Engineering, AI Medical Devices, AI Product, and AI Research & Data Science.
• Present clinical findings and recommendations to cross-functional stakeholders to support product design and development discussions.

• Stakeholder & Site Engagement: Lead interactions with clinical investigators, trial sites, CROs, and other external research partners, escalating to Clinical Product Design Managers when needed.
• Participate in site visits, user observations, and data collection activities as required.
• Gather structured clinician and user feedback to inform clinical research and product improvement.
• Enable the integration of SaMD into clinical practice and ensure the device functions as intended, including conducting site training and owning device training materials.
• Ensure activities conducted with KOLs and research sites are within contractual scope and documented in accordance with internal processes.

• Quality, Compliance & Best Practice: Ensure all relevant activities are conducted in accordance with internal policies, external regulations, and ethical standards, and report deviations to senior leadership.
• Create and support ethical approval applications.
• Maintain accurate and complete study documentation.
• Contribute to the refinement of internal templates, tools, and best practices for clinical research execution.

Qualifications:

• Undergraduate degree (or equivalent) in a biomedical, scientific, or statistical discipline.
• Good Clinical Practice Certification.

Experience:

• Essential: Minimum six years’ experience conducting clinical research, which may include doctoral or equivalent research experience.
• Demonstrated expertise in clinical study design and execution, protocol and report writing, and clinical data interpretation and synthesis.
• Working knowledge of FDA, EU MDR and UKCA clinical evidence requirements, ISO 14155, GDPR, and research governance frameworks.
• Experience working in cross-functional teams.
• Experience supporting evaluations of medical devices and/or Software as a Medical Device, including AI‑based technologies.

• Desirable: Experience supporting multi‑region or global clinical studies.
• Direct experience in endoscopy or related procedural specialities.
• Experience conducting research in a hospital setting and managing hospital research staff.

At Odin Vision we believe that diversity is an important contributor to our success and long-term company goals. Diversity in our teams can contribute to innovations and creativity and increase our ability to cope with change. Odin Vision is committed to encouraging equality, diversity and inclusion among our workforce, and eliminating unlawful discrimination. The aim is for our workforce to be truly representative of all sections of society and our customers, and for each employee to feel respected and able to give their best.