Field Clinical Engineer

🕒 Setembro 25

🇺🇸 Estados Unidos – Remoto (EUA)

💵 $130.000 - $180.000 / ano

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

👷🏻‍♀️ Engenheiro

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EBR Systems, Inc.

SiteLinkedInTodas as Vagas

51 - 200 funcionários

🏭 Manufatura

🏥 Saúde

🧬 Biotecnologia

Manufacturing • Healthcare • Biotechnology

A EBR Systems, Inc. está empenhada em oferecer tratamento superior para milhões de pacientes que sofrem de doenças do ritmo cardíaco, desenvolvendo terapias seguras, clinicamente superiores, econômicas e confiáveis, utilizando estimulação cardíaca sem fio. O produto inicial da empresa, o sistema WiSE® CRT, é um dispositivo médico pioneiro, desenvolvido para superar as limitações da Terapia de Ressincronização Cardíaca (CRT) tradicional em pacientes com insuficiência cardíaca, eliminando a necessidade de um eletrodo no ventrículo esquerdo do coração e as complicações associadas a esse eletrodo. ATENÇÃO: Dispositivo em Investigação. Limitado pela lei dos EUA ao uso investigacional somente.

Descrição

• Support clinical study execution, including recruitment, site start-up, enrollment, and follow-up visits • Provide hands-on clinical, technical, and educational support at study sites • Train and educate physicians, coordinators, and staff on WiSE System use and study procedures • Build and refine processes that enhance site efficiency • Troubleshoot procedural or device-related issues and relay feedback to internal teams • Contribute to educational content, investigator meetings, and continuous improvement initiatives • Ensure compliance with clinical study protocols, Good Clinical Practice, and regulatory requirements • Build relationships with investigators and site staff as liaison between clinical sites and EBR Systems teams • Provide engineering, education, and clinical support for field inquiries • Support clinical monitoring and data collection activities • Mentor and onboard new Field Clinical Engineers • Collaborate with Commercial, Clinical Operations, Data Management, Quality, and Regulatory teams • Develop, review, and maintain site manuals, training materials, and study tools • Participate in site initiation visits, mock implants, and readiness assessments • Support data integrity, query resolution, and timely, accurate data entry • Represent the company at scientific meetings and congresses • Track site and program performance metrics and provide field-based insights • Provide mentorship and guidance to Field Clinical Engineers or contracted clinical support staff • Coordinate site coverage schedules and serve as an escalation point for site-related issues • Provide management feedback on field team performance and study support improvements

🎯 Requisitos

• Bachelor’s degree in Engineering, Biomedical Sciences, Nursing, or a related field • Minimum 5 years of experience in cardiac rhythm management (CRM) or electrophysiology required • Strong knowledge of implantable cardiac devices and heart failure therapies • Minimum 2 years of experience in clinical research, including coordinating multi-center trials with established technical expertise and knowledge • Experience in presenting, writing and teaching clinical and medical information • Experience with group presentations and hands-on experience with Cardiac Rhythm Management products • Ability to work effectively with Clinical Operations, Medical Affairs, Commercial, R&D, Quality, Regulatory, technical specialists, and external stakeholders • Compliance with clinical study protocols and ability to identify and escalate areas of concern • Expertise in CRM and EP clinical procedures, including pacing and defibrillation systems • Ability to support complex clinical trials across multiple centers with high travel demands • Strong communication and interpersonal skills • Proficiency in clinical data collection, protocol adherence, and troubleshooting • Ability to work independently in high-pressure procedural environments • Excellent written and verbal communication skills and proficiency in medical terminology • Clinical Research experience in Medical Device • Experience coordinating multi-center Cardiology trials • Knowledge of Good Clinical Practices and trials, including feasibility IDE and post-market studies • Flexibility to travel frequently and adjust to dynamic schedules • Must reside within the assigned U.S. territory, preferably in the Boston, Baltimore/D.C., Chicago, New York, or Philadelphia areas • Must live within one hour of a major commercial airport • Ability to travel up to 75–85% domestically • Ability to stand, walk, sit, talk, hear, use hands, reach, stoop, kneel, bend, crouch, and lift up to 20 pounds • Required vision abilities include close, distance, depth, color vision, and focus adjustment

🏖️ Benefícios

• Competitive compensation • Equity • Comprehensive benefits • Generous PTO • Medical, dental, and vision insurance provided at no cost for employee-only coverage • 401(k) matching plan • Paid Time Off – starting at 3 weeks per year • Competitive salary with opportunities for career growth • Employee stock options • Life & AD&D and long-term disability insurance • Education assistance • Voluntary commuter benefits and pet insurance • Weekly company lunches and occasional happy hour events • Meaningful work and much more!

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