Senior Project Manager, Clinical Affairs

Company Description

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.

Job Description

Primary Function of Position:

The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D, Regulatory Affairs (RA), Clinical Development Engineering, Quality, and Business Unit PMOs. This role brings disciplined structure, cross-functional coordination, and strategic oversight to high-priority clinical affairs initiatives. Responsibilities include providing project management support and cross-functional coordination—within Clinical Affairs and with enterprise stakeholders—through the planning and execution of clinical studies (e.g., FHUs and IDE studies) and coordinating Clinical Evaluations to support MDR and other global  submissions. The Senior Project Manager is accountable for building and sustaining effective collaboration across stakeholders to ensure Clinical Affairs deliverables are completed successfully and on time.

An ideal candidate brings deep familiarity with medical device development lifecycle as well as clinical lifecycle management, providing tactical guidance for execution frameworks that translate Clinical Affairs objectives into actionable plans, including development roadmaps, governance forums, prioritization, and alignment with business units and other key stakeholders. The role also requires hands-on management of project risks , troubleshooting execution challenges, coordinating internal and external activities, and ensuring milestones are achieved on time and within scope. Examples include developing bottom-up schedules, identifying critical path activities, maintaining risk registers, and leading detailed project reviews to drive continuous improvement.

Additionally, this role supports development of Clinical Affairs tools and operating mechanisms, including project dashboards, capacity and resource planning, and other processes needed to improve visibility, planning, and execution across the function.

Roles and Responsibilities:

• Project Planning & Oversight:

  • Lead  project planning, initiation of Clinical Affairs activities across clinical studies and clinical dossier deliverables, ensuring alignment to program milestones and regulatory expectations.

  • Develop and maintain integrated project plans that define scope, timelines, dependencies, resourcing, and deliverables for key Clinical Affairs workstreams.

  • Partner with cross-functional teams (R&D, Regulatory, Business Units, Clinical Development Engineering, Quality, and PMO) to align dependencies to support Clinical Affairs deliverables to the broader product development lifecycle.

  • Track progress against milestones for clinical trials and global clinical dossier submissions (e.g., EU Clinical Evaluation Reports [CERs]), including metric reporting and portfolio status summaries.

  • Facilitate routine cross-functional meetings; provide clear status updates, document decisions, and capture/drive action items to closure.

• Clinical Affairs Internal Coordination:

  • Coordinate activities within clinical affairs with subfunctions such as  clinical operation, Clinical Data Management, Biostatistics, and Medical Sciences to ensure timely, consistent execution of study and submission deliverables.

  • Create and maintain tracking tools (dashboards, action logs, and schedules) to monitor study/submission progress, highlight risks and dependencies, and support proactive decision-making.

  • Support budget and timeline adherence by identifying resource constraints early, escalating as needed, and driving mitigation plans