Associate Clinical Scientist / Clinical Scientist
ResearchEd
Google Cloud Platform
Field Clinical Engineer
EBR Systems, Inc.
full-time
Posted on:
Origin: • 🇺🇸 United States
Visit company websiteSalary
💰 $130,000 - $180,000 per year
Job Level
Mid-LevelSenior
Tech Stack
Google Cloud Platform
About the role
- 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.
- 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 EBR Systems’ clinical, regulatory, and R&D teams on site feedback and product insights.
- Provide engineering, education and clinical support in response to field inquiries on as-needed basis.
- Support clinical monitoring and data collection activities at assigned sites, including data quality efforts and query resolution.
- Mentor and onboard new FCE team members; may serve as regional lead coordinating site coverage schedules and acting as first escalation point.
- Partner with Commercial, Clinical Operations, Data Management, Quality, and Regulatory teams to align site activities with broader study goals.
- Participate in site initiation visits, mock implants, and readiness assessments; represent company at scientific meetings and congresses.
Requirements
- 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.
- Minimum 2 years of experience in clinical research including coordinating multi-center trials with established technical expertise and knowledge.
- Strong knowledge of implantable cardiac devices and heart failure therapies.
- Experience in presenting, writing and teaching clinical and medical information.
- Experience with group presentations and hands-on experience with Cardiac Rhythm Management products.
- Knowledge of Good Clinical Practices and trials, including feasibility IDE and post- market studies.
- Ability to work effectively with internal groups such as Clinical Operations, Medical Affairs, Commercial, R&D, Quality, Regulatory, technical specialists, and external stakeholders to achieve assigned goals.
- Ensure compliance with clinical study protocol, and identifying areas of concern and escalating when appropriate.
- Strong communication and interpersonal skills, with proficiency in medical terminology.
- Demonstrated ability to work independently in high-pressure procedural environments.
- Flexibility to travel frequently and adjust to dynamic schedules; ability to travel up to 75-85% domestically.
- Physical requirements: stand, walk and sit; talk or hear; use hands to finger, handle or feel objects or controls; reach with hands and arms; stoop, kneel, bend, crouch; lift up to 20 pounds; close vision, distance vision, depth perception, color vision and the ability to adjust focus.
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