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Field Clinical Engineer

Salvia BioElectronics Inc.
Hybrid

About The Position

As a Field Clinical Engineer at Salvia BioElectronics, you’ll play a key role in the success of our clinical trials. From supporting implant procedures and patient follow-ups to ensuring smooth trial operations, your work will help bring innovative neuromodulation therapies closer to people living with migraine. Every step you take contributes directly to transforming lives.

Requirements

  • Minimum 2 years’ experience as a Field Clinical Specialist/Engineer specifically with implantable neurostimulation devices and therapy programming for pain or headache patients
  • Min 1 year experience in pre-market implantable neuromodulation device studies managing clinical trial sites
  • Degree in Biomedical Engineering, Nursing, Neuroscience, Life Sciences or related field. Or equivalent experience in patient facing roles
  • Strong patient focus with an empathetic and compassionate approach
  • Team player with a positive, proactive, constructive, and problem-solving attitude
  • Able to work independently
  • Highly organized to manage frequent and changing travel schedule
  • Ability to travel extensively, approximately 75 percentage
  • Living in Southern California or Dallas Fort Worth Area

Responsibilities

  • Build and maintain strong relationships with clinical site staff, investigator, referring neurologists, and other healthcare professionals
  • Provide technical support during implantation procedure and follow up visits, including programming
  • Deliver ongoing technical training on the implantation and use of the Salvia products
  • Troubleshoot and resolve issues with devices in the field, in collaboration with the in-house technical team
  • Organize and coordinate cadaver training workshops on the surgical procedure
  • Support clinical trial activities, including Site Interest Visits, Site Initiation Visits, training on clinical protocols, procedures and investigational products
  • Connect with potential clinical investigators to identify clinical needs and research interests
  • Actively and timely complaint and/or safety reporting (adverse events, device deficiencies)
  • Actively collect and provide feedback on user experience
  • Ensure compliance with the applicable, local, and national regulations

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