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Research Science Management

Intuitive

Sunnyvale, CARemotePosted 1 day ago$132,000 - $223,500/year
Full TimeSenior LevelResearch & ScientistMedical Device
Original posting ↗

Summary

The purpose of this role is to serve as a Scientific Research Program Manager (SRPM) supporting evidence strategy and research programs across Intuitive Surgical's da Vinci platforms, products, and services. The SRPM will collaborate with cross-functional stakeholders to identify evidence needs and priorities and support the development and execution of evidence-generation strategies and research plans. This role oversees the initiation, progress, and conduct of evidence-generation studies, including those conducted by internal scientific teams, Intuitive-sponsored studies, and studies conducted in collaboration with external research partners.

Job description

Primary Function of Position

The purpose of this role is to serve as a Scientific Research Program Manager (SRPM) supporting evidence strategy and research programs across Intuitive Surgical's da Vinci platforms, products, and services. The SRPM will collaborate with cross-functional stakeholders to identify evidence needs and priorities and support the development and execution of evidence-generation strategies and research plans. This role oversees the initiation, progress, and conduct of evidence-generation studies, including those conducted by internal scientific teams, Intuitive-sponsored studies, and studies conducted in collaboration with external research partners.

Essential Job Duties

  • Collaborate with da Vinci and Multiport program leaders and cross-functional evidence stakeholders to identify evidence requirements and gaps, align on evidence priorities, and develop evidence strategies and plans.
  • Manage and execute a portfolio of internal and external collaborative research studies and evidence-generation activities for Intuitive Surgical's da Vinci platforms, products, and services.
  • Manage research studies across the study lifecycle, including project development, budgeting, investigator selection, analysis of potential participant recruitment, preparation of study-related documents (e.g., protocols, case report forms, informed consents, research agreements), and management of Institutional Review Board and/or Ethics Committee submissions.
  • Collaborate with data management professionals and statisticians as needed; maintain required study documentation; and plan and manage project timelines and budgets.
  • Proactively identify and communicate project concerns, issues, and delays; develop risk assessments and contingency plans; and prepare project status updates, presentations, and reports.
  • Manage publication development, submission, and responses to peer review related to research studies.
  • Ensure compliance with corporate requirements (e.g., SOPs) and applicable regulatory requirements (e.g., GCP and U.S. and international guidelines), and maintain audit readiness.
  • Manage Contract Research Organizations (CROs) and independent research service providers, including partner identification, contract or statement-of-work development, and stakeholder management.
  • Build, nurture, and maintain relationships with external research partners and stakeholders, including surgeon key opinion leaders, operating room staff, hospital and health system leaders, and industry partners.

Qualifications

  • Bachelor's degree or equivalent in life sciences, medicine, medical sciences, engineering, computer science, data science, or a related field.
  • Minimum five years of experience in an academic setting or healthcare technology industry in a clinical affairs or scientific research function, with evidence of full project management responsibility.
  • Knowledge of applicable clinical research and medical device regulations and guidelines, including GCP, ISO 14155, MEDDEV, MDR, and data protection requirements.
  • Experience developing research protocols and case report forms (CRFs).
  • Strong organizational skills and ability to manage multiple projects with competing priorities.
  • Strong communication, interpersonal, and negotiation skills.
  • Strong quantitative and literature analysis skills.
  • Ability to manage CROs, external consultants, research coordinators, or other research staff.
  • Strong problem-solving skills and initiative; English-language proficiency required.
  • Ability to travel 25%-50% of the time.

Preferred Skills and Experience

  • Graduate degree in life sciences, medicine, medical sciences, engineering, computer science, data science, or a related field.
  • Five years of experience in the management of research, including clinical research management experience in both academic/hospital and industry settings.
  • Experience with studies of health information technologies, including artificial intelligence.
  • Experience publishing research in an academic or industry capacity.
  • Proficiency in a second language.

Requirements

  • Bachelor's degree or equivalent in life sciences, medicine, medical sciences, engineering, computer science, data science, or a related field
  • Minimum five years of experience in an academic setting or healthcare technology industry in a clinical affairs or scientific research function
  • Evidence of full project management responsibility
  • Knowledge of clinical research and medical device regulations and guidelines including GCP, ISO 14155, MEDDEV, MDR, and data protection requirements
  • Experience developing research protocols and case report forms (CRFs)
  • Strong organizational skills and ability to manage multiple projects with competing priorities
  • Minimum of three to five research projects across different surgical disciplines and/or products
  • Strong communication, interpersonal, and negotiation skills
  • Ability to manage work autonomously and collaborate across teams
  • Strong quantitative and literature analysis skills
  • Ability to manage CROs, external consultants, research coordinators, or other research staff
  • Strong problem-solving skills and initiative
  • English-language proficiency required
  • Ability to travel 25%-50% of the time

Benefits

  • Health Insurance
  • Equity
  • Incentives
  • Competitive Compensation

Company overview

Intuitive Surgical, Inc., commonly known as Intuitive, is a global technology leader in minimally invasive care and the pioneer of robotic-assisted surgery. Founded in 1995 and headquartered in Sunnyvale, California, the company has revolutionized surgical procedures through its flagship da Vinci Surgical System and Ion endoluminal system. As a publicly traded company on NASDAQ (ISRG), Intuitive has established itself as the dominant player in robotic surgery, with over 15,000 employees worldwide and an installed base of thousands of surgical systems across more than 60 countries. The company's innovative platforms enable surgeons to perform complex procedures with enhanced precision, flexibility, and control through minimally invasive techniques. Intuitive's technology portfolio includes advanced vision systems, wristed instruments, and intelligent software that work together to optimize surgical outcomes. The company continues to expand its product offerings and geographic presence while maintaining a strong focus on clinical evidence, physician training, and patient safety. With annual revenues exceeding $8 billion, Intuitive represents a transformative force in modern healthcare, driving the adoption of robotic-assisted procedures across multiple surgical specialties including urology, gynecology, general surgery, and thoracic surgery.

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