Intuitive Autonomy
Sr Director, Translational Research Scientist - MD/PhD
Sunnyvale, CA, United States · Director
Sponsorship not specifiedDetected 6 days ago
GCPData AnalysisProduct ManagementProduct StrategyPharmacologyFDA RegulatoryMedical DevicesResearchExperimental DesignAnimal StudiesLeadershipCommunicationCollaborationMentoringPublic SpeakingOrganizational SkillsGxP
About the role
- Nearly 30 years later, that question still fuels everything we do at Intuitive.
- As a global leader in robotic-assisted surgery and minimally invasive care, our technologies-like the da Vinci surgical system and Ion -have transformed how care is delivered for millions of patients worldwide.
Responsibilities
- Develop and validate experimental models, assays, and protocols that characterize clinical outcomes and support regulatory filings
- Manage data integrity and study documentation per requirements including GLP (Good Laboratory Practice)/GCP (Good Clinical Practice) best practices for research.
- Build and sustain strongdeep, trusted relationships with collaborating investigators, labs and study sites.
- Maintain awareness of study progress with collaborating labs.
- Establish and maintain open lines of communication with principal investigators and collaborating scientists.
- Convert clinical findings into actionable inputs for product development and design evolution.
- Support validation of safety and efficacy for products not yet on label across multiple trials.
- Collaborate on which investigators and KOLs to prioritize, ensuring coordinated outreach and consistent communication.
- Support harmony between clinical trial activity and existing commercial product presence while maintaining strict compliance boundaries for not-on-label products.
- Collaborate closely with strategic alliance partners conducting sponsored studies.
Requirements
- Ability to analyze complex biological and engineering data, produce study reports, and present findings to technical and nontechnical stakeholders.
Nice to have
- Experience with GLP-compliant study execution or working with CROs under GLP frameworks.
- Experience establishing external academic or CRO partnerships and negotiating study agreements.
- Relocation is preferred but not required for this role.
- Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19.
- Details can vary by role.
- Intuitive is an Equal Opportunity Employer.
- Mandatory Notices
- For any Intuitive
Skills
- It started with a simple idea: what if surgery could be less invasive and recovery less painful?
Benefits
- These may include in vitro, ex vivo, and/or in vivo studies to evaluate mechanism of action, performance, and safety of medical devices
- Analyze and interpret study data then synthesize findings into study reports focusing on implications for medical device development and clinical study design.
- Serve as a trusted collaborator to investigators and site teams, capable of discussing the underlying science and potential implications for medical device design as well as clinical implications..
- Identify and characterize patient subgroups most likely to benefit, including anatomical, physiological, and disease-specific factors.
Company info
- Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S.
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