Research Engineer

About Nevro: Nevro (NYSE: NVRO)is a global medical device company headquartered in Redwood City, California. We are focused on providing innovative products that improve the quality of life of patients suffering from debilitating chronic pain.We started with a simple mission to help more patients suffering from chronic pain. At each stage of development, our research was subject to the highest levels of scientific rigor, resulting in a new therapy that has impacted the lives of over 70,000 patients around the world.Nevro has developed and commercialized the Senza spinal cord stimulation (SCS) system, an evidence-based, non-pharmacologic neuromodulation platform for the treatment of chronic pain. HF10 therapy has demonstrated the ability to reduce or eliminate opioids in 65% of patients across six peer-reviewed clinical studies. The Senza System, Senza II System, and the Senza Omnia System are the only SCS systems that deliver Nevro's proprietary HF10 therapy.

Job Summary & Responsibilities: The Research Engineer is responsible for investigating and implementing the technical and clinical vision of the advanced technology group. The engineer will also research and investigate disruptive technical and clinical opportunities including developing clinical models of efficacy. He/she will be responsible for the tactical implementation of the program and projects within the group. Lastly, he/she will also be responsible for assisting in defining market opportunities.Investigate novel and disruptive technologies and clinical therapies with the objective to expand Nevros therapyAssists in the exploration and evaluation of external technical and clinical opportunities and performing assessments, recommendations and technical due diligenceWorks closely with other team members in designing experimental protocols, as well as the conducting and monitoring these research projects, and interpretation of resultsParticipates in the development and writing of integrated reports and preparation of presentations and manuscripts of scientific meetings and technical journalsParticipates in design and writing of protocols, case report forms and informed consent forms for clinical trialsPerforms a variety of analysis in the collection, verification, analysis, documentation and interpretation of research dataEvaluates and interprets collected data, and prepares presentations, reports and analyses describing progress, trends, and recommendations or conclusionsIdentify, assess, recommend, and integrate novel technologies and/or clinical therapiesConduct descriptive and exploratory analysis of technical and clinical data Define statistical tests and methods for both evaluating and generating statistical hypothesesWork cross-functionally (e.g., business development, engineering, marketing, clinical affairs, quality, and legal) as needed to assess potential opportunities Other duties as assigned.

Role Requirements: Masters or Ph.D degree in biomedical science and/or electrical engineering required; an M.D. or advanced degree in a technical field and/or MBA preferred5+ years experience in the medical fieldEquivalent work experience may be substituted for education requirement.

Skills and Knowledge: Demonstrated ability to deliver on milestone based programs and projectsDemonstrated understanding of medical technologies and clinical therapiesDemonstrated knowledge and understanding of human physiology and anatomyDemonstrated knowledge and understanding of human neurophysiology and neuroanatomyDemonstrated ability to implement technical and clinical solutionsDemonstrated experience with observational studies and patient reported outcomes Demonstrated ability to determine market drivers and conduct market researchDemonstrated astuteness in identifying and understanding meaningful intellectual propertyExperience interfacing with external partners (e.g., physicians, consultants, companies, academia)Demonstrated interpersonal and communication skills #LS-TS1

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