Field Clinical Engineer - East

Description About E  Systems

At E  Systems, we're not imagining the future of cardiac care. We're building it. We are the team behind the world's first FDA-approved leadless left ventricular endocardial pacing device for heart failure. It's a breakthrough that's redefining what's possible, and it's just the beginning.

Based in Silicon Valley, we're advancing the WiSE System, a first-of-its-kind device in cardiac rhythm management. Your work here has a direct line to patients whose lives depend on what we build. We hire people who want to solve hard problems and who care about getting it right.

We invest in our people as much as our technology. Expect a collaborative, transparent culture, real career growth in a fast-moving startup, competitive compensation, equity, comprehensive benefits, and generous PTO.

If you want your work to matter, E  is where you belong.

The Field Clinical Engineer (FCE) plays a critical role in supporting E  Systems’ clinical research programs in the field. This role provides technical, clinical, and educational support to physicians and research staff during study visits in ongoing clinical studies. The FCE serves as a clinical interface between the company and medical community, ensuring adherence to study protocols, supporting high-quality data collection, and advancing patient safety and outcomes.

This is a remote field-based position within an assigned U.S. region. Candidates must reside within the assigned territory, preferably in Boston, Baltimore/D.C, Chicago, New York or Philadelphia areas, and live within one hour of a major commercial airport.

• Support all aspects of clinical study execution, including recruitment, site start-up, enrollment, and follow-up visits at assigned sites.
• Provide hands‑on clinical, technical, and educational support at study sites to ensure protocol adherence and high-quality data collection.
• Serve as the field subject matter expert on the WiSE System, training and educating physicians, coordinators, and staff on device use and study procedures.
• Works independently, applying best practices to build and refine processes that enhance site efficiency in study-related activities, while continually seeking opportunities for improvement.
• Troubleshoot procedural or device‑related issues and relay timely feedback to internal teams.
• Develop and refine processes that improve site efficiency and streamline study‑related activities.
• Contribute to educational content, investigator meetings, and continuous improvement initiatives by sharing clinical insights and market feedback.
• Ensure compliance with clinical study protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Build strong relationships with investigators and site staff, acting as a trusted liaison between clinical sites and E  Systems’ clinical, regulatory, and R&D teams on site feedback and product insights.
• Provides engineering, education and clinical support in response to field inquiries on as‑needed basis.
• Demonstrates ability to build and sustain credible business relationships with customers and shares product expertise accordingly.
• Support clinical monitoring and data collection activities at assigned sites.

• Operates with a high degree of independence and initiative; able to manage complex priorities with minimal supervision.
• Strong program management skills with the ability to organize, plan, and drive multiple site activities forward.
• Builds trust and credibility quickly with physicians, coordinators, and stakeholders.
• Highly motivated self‑starter who thrives in dynamic environments with significant travel.
• Collaborative team player who…