Field Clinical Engineer

🕒 vor 1 Monat

🇺🇸 Vereinigte Staaten – Remote

💵 $130.000 - $180.000 / Jahr

⏰ Vollzeit

🟡 Mittelstufe

🟠 Senior

👷🏻‍♀️ Ingenieur

👻 Geisterscore 3%

Was es bedeutet: die Wahrscheinlichkeit, dass für diese Stelle niemand wirklich einstellt.So liest du es: 60 % oder höher heißt, wir halten das für einen Geisterjob. Niedrigere Werte sind weniger bedenklich.Warum dieser Wert:

• Seit 46 Tagen offen.
• Stellen bei diesem Unternehmen werden meist in 38 Tagen besetzt.

Jetzt Bewerben

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EBR Systems, Inc.

WebsiteLinkedInAlle Stellen

51 - 200 Mitarbeiter

🏭 Fertigung

🏥 Gesundheitswesen

🧬 Biotechnologie

Manufacturing • Healthcare • Biotechnology

EBR Systems, Inc. hat es sich zur Aufgabe gemacht, überlegene Behandlungen für Millionen von Patienten mit Herzrhythmusstörungen bereitzustellen, indem sichere, klinisch überlegene, kosteneffektive und zuverlässige Therapien mit drahtloser Herzstimulation entwickelt werden. Das erste Produkt des Unternehmens, das WiSE® CRT-System, ist ein neuartiges medizinisches Gerät, das entwickelt wurde, um die Einschränkungen der traditionellen Kardiale Resynchronisationstherapie (CRT) bei Herzinsuffizienzpatienten zu überwinden, indem die Notwendigkeit einer Elektrode zur linken Herzkammer und die damit verbundenen Komplikationen beseitigt werden. ACHTUNG: Untersuchungsgerät. In den USA gesetzlich auf den Gebrauch zu Untersuchungszwecken beschränkt.

Beschreibung

• 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

🎯 Anforderungen

• 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

🏖️ Vorteile

• 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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