

New · posted Nov 14
Intuitive · Medical Devices
Clinical Research Intern
- Sunnyvale, CA
- On-site
- Internship
- Associate & Specialist
The role
It started with a simple idea: what if surgery could be less invasive and recovery less painful? 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.
We’re a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world.
The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful—because every improvement we make has the potential to change a life.
If you’re ready to contribute to something bigger than yourself and help transform the future of healthcare, you’ll find your purpose here.
Primary Function of Position
The Clinical Research Intern will join Intuitive's Future Forward Advanced Research team for a 10–12 week summer internship, reporting to a Senior Clinical Research Scientist within Future Forward. The intern will contribute directly to early-stage product development for a novel technology platform, applying clinical and scientific expertise to support product strategy, clinical evidence generation planning, and market opportunity evaluation. Working alongside cross-functional team members in engineering, translational science, medical affairs, and product management, the intern will help de-risk key clinical and strategic uncertainties for an early technology in development. The internship culminates in a final presentation to leadership and cross-functional partners.
What you need
Required Skills and Experience
· Demonstrated ability to critically evaluate clinical literature and synthesize findings into actionable strategic insights.
· Experience with clinical study design concepts or clinical trial planning.
· Strong analytical and problem-solving skills with the ability to develop and test clinical hypotheses.
· Experience or training in needs-based innovation, clinical immersion, or translational research (e.g., Biodesign, clinical fellowships, or equivalent).
· Strong written and verbal communication skills, with the ability to translate complex clinical and scientific concepts for diverse audiences including engineering and business teams.
· Comfortable working on defined deliverables under the guidance of senior team members, with the independence to drive them to completion within the internship period.
· Intellectual curiosity and comfort with ambiguity; this team works on problems that are not yet fully defined.
Required Education and Training
· Current enrollment in a Medicine (MD), Bioengineering, Biomedical Sciences, or related degree-seeking program at the Doctorate (MD or PhD) level.
· Master's level students with specific relevant experience in clinical research, Biodesign / needs-based innovation training, or medical device product development may also be considered.
Working Conditions (As applicable - Any physical requirements for the job. If not applicable, state “none”)
None
Preferred Skills and Experience (As applicable - Specific skills, knowledge, and experience that are not required to perform the job, but are desirable to have)
· Completion of or current enrollment in a Biodesign or equivalent needs-based innovation program (e.g., Stanford Biodesign, Georgia Tech, Johns Hopkins, or similar).
· Experience in upstream product management, product strategy, or product development within medical devices or healthcare technology.
· Clinical experience in a surgical or interventional specialty (e.g., through residency, clinical rotations, or research fellowships).
· Familiarity with regulatory pathways (e.g., 510(k), De Novo, PMA) and design controls for medical devices.
· Experience with health economics, market sizing, or reimbursement analysis.
· Intellectual property awareness or experience contributing to patent disclosures.
· Peer-reviewed publications or congress abstracts in relevant clinical or engineering domains.
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.
U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status.
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. Government on your behalf (note: the government’s licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“TCP”) (note: typically adds 2 weeks to the hiring process).
For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee’s start date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes.
We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.
Accommodation & Accessibility Notice:
We provide market-competitive compensation packages, inclusive of base pay (paid at an hourly rate), benefits, and a housing allowance. It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including relevant skills and experience for this internship, degree-seeking academic program (PhD, Master’s, Bachelor’s, etc), year in school, and location. The hourly rate is prorated against the intern program salaries listed and total program compensation will be based on internship duration.
University Hiring Program Eligibility Requirements
· University Enrollment: Must be currently enrolled in and returning to an accredited degree-seeking academic program after the internship.
· Internship Work Period: Must be available to work full-time (approximately 40 hours per week) during a 10-12 week period starting May or June. Specific start dates are shared during the recruiting process.
What you'll do
Clinical Evidence Strategy: Develop and refine clinical evidence generation strategies for an early-stage technology platform, including identifying key clinical endpoints, target patient populations, and study design considerations.
Literature Review & Outcomes Research: Conduct targeted literature reviews and clinical outcomes research to benchmark the technology against standard of care, identify evidence gaps, and support clinical trial planning activities.
Scientific De-Risking: Collaborate with translational science teams to identify, prioritize, and de-risk key scientific and clinical risks for the technology under development; contribute to de-risking plans, experimental design, and milestone definitions.
Product Development: Partner with cross-functional teams, including engineering, medical affairs, and product management, to support early project de-risking activities, align clinical requirements with technical feasibility, and contribute to risk mitigation plans.
Product Strategy & Market Opportunity Evaluation: Evaluate expansion market opportunities by analyzing disease-state epidemiology, procedure volumes, competitive landscapes, and unmet clinical needs for adjacent or new clinical applications. Translate clinical insights into product and market requirements, contributing to upstream product strategy, clinical value propositions, and market positioning. Potential participation in clinical observations, physician interviews, or voice-of-customer sessions.
Communication & Deliverables: Summarize findings in clear visualizations, written deliverables, and presentations; deliver a final presentation to leadership and cross-functional partners.
Pay and benefits
Intuitive didn't publish pay for this role
Try the salary calculator.
Market-competitive compensation
Housing allowance
Where you'll work
Sunnyvale, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in Sunnyvale, CAEqual opportunity, accessibility and legal noticesIntuitive's statements, word for word
Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.
Intuitive is committed to providing reasonable accommodations to qualified individuals with disabilities. If you require assistance or an accommodation during any part of the application or interview process, please contact People Services at [email protected].
Job intelligence
The context around this role
Live data · November 14, 2026
Career trajectory
Where this role sits in Clinical Affairs
The general path across 26 open Clinical Affairs roles on Regulatory Jobs, with the titles they carry most. Not Intuitive's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 40 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership12
- Clinical trial conduct4
- GMP and compliance1
- Lab testing and methods1
- Documentation and SOPs1
- Regulatory submissions1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Affairs work in medical devices, led by the three this posting names, each linked to the agency or standards body that publishes it.
- FDAFDA 510(k)(official source, opens in a new tab)Premarket notification: showing substantial equivalence to a legally marketed deviceNamed in the posting
- FDA21 CFR Part 814(official source, opens in a new tab)Premarket approval of class III medical devicesNamed in the posting
- FDAFDA De Novo(official source, opens in a new tab)Classification requests for novel low- to moderate-risk devicesNamed in the posting
- ISOISO 14155(official source, opens in a new tab)Good clinical practice for clinical investigations of medical devices
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
- EUMDCG guidance(official source, opens in a new tab)The Medical Device Coordination Group's endorsed guidance on applying the MDR and IVDR
- FDA21 CFR Part 812(official source, opens in a new tab)Investigational device exemptions for clinical studies of devices
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- FDA21 CFR Part 56(official source, opens in a new tab)Institutional review boards for FDA-regulated clinical investigations
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trials
- FDAFDA Q-Submission Program(official source, opens in a new tab)Pre-Submissions and meetings with FDA on device submissions
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
From Regulatory News
Company hiring pulse
Intuitive on Regulatory Jobs
- 34
- Open roles
- 34
- Distinct roles
- 5
- Locations
By discipline
- Quality14 40%
- Clinical11 31%
- Regulatory10 29%
By level
- Senior & Principal20 57%
- Manager8 23%
- Associate & Specialist6 17%
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Clinical Research Intern at Intuitive
Open until filled.


