Scientific Research Program Manager

Job not on LinkedIn

🔥 1 minute ago

🏄 California – Remote

🏄 California – Remote

💵 $132k - $223.5k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

📋 Program Manager

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Intuitive

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1995

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Intuitive is a company known for its innovative surgical technologies, including the da Vinci Surgical Systems which are used for minimally invasive procedures. With three decades of demonstrated performance, Intuitive focuses on advancing healthcare by providing structured and measurable technology training pathways for surgeons, physicians, and OR care teams. Their vision is to improve patient outcomes through less invasive surgical care. Intuitive also offers a visual media platform for collaboration and learning, known as the Da Vinci Hub, and the Simnow platform for surgical training. The company is involved in ongoing innovation to explore new possibilities in surgical care.

📋 Description

• Serve as Scientific Research Program Manager for the da Vinci Cardiac Surgery Program • Develop evidence-generation strategy for the Cardiac Surgery Program • Support research projects demonstrating the performance and impact of Intuitive Surgical's da Vinci platforms, products, and services in the United States and globally • Oversee initiation, progress, and conduct of internal, sponsored, and externally collaborative evidence-generation studies • Collaborate with program leaders and cross-functional stakeholders to identify evidence gaps, prioritize evidence, and develop evidence-generation plans • Manage a portfolio of internal and external collaborative research studies and evidence-generation activities • Manage studies across the full lifecycle, including development, budgeting, investigator selection, participant recruitment analysis, study documents, and IRB/Ethics Committee submissions • Collaborate with data management professionals and statisticians; maintain study documentation; and manage timelines and budgets • Identify and communicate project concerns, delays, and risks; develop contingency plans; and prepare status updates, presentations, and reports • Manage publication development, submission, and peer-review responses • Ensure compliance with corporate SOPs, GCP, and U.S. and international regulatory guidelines; maintain audit readiness • Manage CROs and independent research service providers, including partner identification, contracts or statements of work, and stakeholder management • Support development of internal research processes and SOPs • Build and maintain relationships with research partners, surgeon key opinion leaders, hospital stakeholders, professional societies, and healthcare technology partners

🎯 Requirements

• At least five years of experience in an academic setting or healthcare technology industry in a clinical affairs or scientific research function, with 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) • Ability to manage at least three to five research projects across different surgical disciplines and/or products • Strong organizational, communication, interpersonal, negotiation, quantitative, literature analysis, problem-solving, and initiative skills • Ability to manage work autonomously and collaborate across teams • Ability to assess data and scientific literature and review data sets for data quality • Ability to manage CROs, external consultants, research coordinators, or other research staff • English-language proficiency required • Bachelor's degree or equivalent in life sciences, medicine, medical sciences, engineering, computer science, data science, or a related field • Ability to travel 25%-50% of the time • Work may require presence in hospital and surgical/operating room environments • Preferred: graduate degree; five years of research management experience in both academic/hospital and industry settings; health information technology studies including artificial intelligence; research publication experience; proficiency in a second language • May require current proof of vaccination against certain diseases, including COVID-19 • Certain roles may be subject to U.S. export-control licensing or a Technology Control Plan

🏖️ Benefits

• Remote work; employees come onsite when requested by the leader • Market-competitive compensation packages including incentives, benefits, and equity • Reasonable accommodations for qualified individuals with disabilities • Potential vaccination coverage/requirements for certain diseases, including COVID-19 • Equal employment opportunity protections • Fair chance consideration for applicants with arrest and conviction records

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