Sr Clinical Imaging Scientist

Fluorescence Imaging at Intuitive Surgical
The Fluorescence Imaging Team at Intuitive is developing agents designed to work seamlessly with Intuitive's robotic platforms and Firefly imaging technology. The agents have the potential to highlight critical anatomy and disease in real time—giving surgeons clearer information at the moment decisions matter most and helping improve outcomes for patients.
Primary Function of Position
The Senior Clinical Scientist is responsible for supporting the scientific design and execution of clinical evidence-generation activities across Intuitive's fluorescence imaging ecosystem. The role focuses on developing robust clinical endpoints, defining data collection strategies, establishing data quality and monitoring processes, and supporting the generation of evidence used to evaluate imaging agents, software tools, and future ecosystem applications.
The position serves as a bridge between clinical development, data science, engineering, and external partners, helping ensure that scientific questions are translated into clinically meaningful, measurable, and regulatory-defensible outcomes. The successful candidate will combine expertise in clinical research methodology with a strong understanding of diagnostic performance assessment, clinical data interpretation, and evidence generation in support of innovative surgical technologies.
Roles and Responsibilities
Clinical Study Design and Endpoint Development
Support execution of clinical studies evaluating fluorescence imaging agents and ecosystem technologies.
Translate protocol-defined endpoints into operationally executable study procedures and data collection requirements.
Partner with Clinical Development, Data Management, and Biostatistics to ensure endpoint assessments are implemented consistently across sites.
Develop study-specific guidance supporting accurate and reproducible endpoint determination.
Support review of protocols and statistical analysis plans to ensure alignment between study procedures, data collection methods, and endpoint assessments.
Conduct literature reviews and scientific assessments supporting ongoing clinical development activities.
Clinical Data Collection & Quality Strategy
Develop data collection frameworks supporting assessment of imaging performance and clinical outcomes.
Partner with Data Management to design CRFs, edit checks, and data review workflows.
Define procedures for collection of imaging, pathology, surgical, and clinical outcome data.
Establish data quality metrics and review processes to promote completeness, consistency, and protocol compliance.
Identify potential sources of variability, bias, and missing data and recommend mitigation strategies.
Support ongoing review of clinical data throughout study conduct.
Data Monitoring and Evidence Generation
Develop risk-based data monitoring and data review approaches for fluorescence imaging programs.
Conduct scientific review of emerging study data and identify trends requiring further investigation.
Support blinded image review workflows and centralized assessment activities.
Collaborate with Clinical Development and Biostatistics on interpretation of study results.
Assist with database lock activities, clinical study reports, publications, abstracts, and presentations.
Contribute to development of evidence packages supporting clinical, scientific, and business objectives.
AI & Data Science Collaboration
Partner with Data Science and Engineering teams to develop high-quality datasets supporting AI-enabled imaging applications.
Support development of annotation strategies, reference standards, and validation datasets.
Assist in evaluating algorithm performance against established clinical endpoints and reference standards.
Provide clinical and workflow expertise to support future computational and ecosystem initiatives.
Contribute to evidence-generation activities supporting AI-enabled features and third-party ecosystem applications.
Regulatory & Scientific Communication
Author and review scientific content for protocols, study reports, publications, and internal development documents.
Support preparation of materials for regulatory interactions and health authority submissions.
Present scientific findings to internal stakeholders and external collaborators.
Maintain consistency of endpoint definitions and scientific rationale across development documents.
PhD, PharmD, MD, MPH, or MS in biomedical sciences, clinical research, epidemiology, biomedical engineering, or related field.
Minimum 5 years of experience in clinical research, clinical development, medical affairs, diagnostics, medical devices, pharmaceuticals, or related healthcare industries.
Experience supporting clinical study design and endpoint development.
Strong understanding of clinical research methodology and evidence generation.
Experience interpreting clinical and diagnostic performance data.
Familiarity with protocol development, clinical databases, and data review processes.
Ability to work effectively across multidisciplinary teams.
Strong scientific writing, presentation, and communication skills.
Preferred Qualifications
Experience in oncology, surgical oncology, medical imaging, molecular imaging, or fluorescence-guided surgery.
Experience supporting regulatory submissions or health authority interactions.
Familiarity with diagnostic accuracy studies, including sensitivity, specificity, predictive values, and reference standard methodology.
Experience working with imaging datasets, digital pathology, AI/machine learning applications, or quantitative image analysis.
Experience collaborating with software, data science, or engineering teams.
Knowledge of robotic-assisted surgery and image-guided procedures.

Employment type
Full-time

Work arrangement
No