- Assists in the investigate novel, disruptive technologies, and clinical therapies
- Assists in the exploration and evaluation of external technical and clinical opportunities and performing assessments, recommendations and technical due diligence
- Works closely with other team members in designing experimental protocols, as well as the conducting and monitoring these research projects, and interpretation of results
- Participates in the development and writing of integrated reports and preparation of presentations and manuscripts of scientific meetings and technical journals
- Participates in design and writing of protocols, case report forms and informed consent forms for clinical studies
- Performs a variety of analysis in the collection, verification, analysis, documentation and interpretation of research data
- Evaluates and interprets collected data, and prepares presentations, reports and analyses describing progress, trends, and recommendations or conclusions
- Identify, assess, recommend, and integrate novel technologies and/or clinical therapies
- Conduct descriptive and exploratory analysis of technical and clinical data
- Define statistical tests and methods for both evaluating and generating statistical hypotheses
- Work cross-functionally (e.g., business development, engineering, marketing, clinical affairs, quality, and legal) as needed to assess potential opportunities
- Other duties as assigned.
- Masters or Ph.D degree in biomedical and/or electrical engineering required; an M.D. or advanced degree in a technical field and/or MBA preferred
- 5+ years experience in the medical field
- Equivalent work experience may be substituted for education requirement.
- Demonstrated ability to deliver on milestone-based programs and projects
- Demonstrated understanding of medical technologies and clinical therapies
- Demonstrated understanding of quality management systems
- Demonstrated understanding of regulatory processed and policies
- Demonstrated knowledge and understanding of human physiology and anatomy
- Demonstrated knowledge and understanding of human neurophysiology and neuroanatomy
- Demonstrated ability to implement technical and clinical solutions
- Demonstrated experience with observational studies and patient reported outcomes
- Demonstrated astuteness in identifying and understanding meaningful intellectual property
- Demonstrated interpersonal and communication skills
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Research Engineer III - Redwood City, United States - Nevro
Description
About Nevro:
Nevro (NYSE: NVRO) is a global medical device company headquartered in Redwood City, California. We are focused on delivering comprehensive, life-changing solutions that continue to set the standard for enduring patient outcomes in chronic pain treatment. The company started with a simple mission to help more patients suffering from debilitating pain and developed its proprietary 10 kHz Therapy, an evidence-based, non-pharmacologic innovation that has impacted the lives of more than 100,000 patients globally.
Nevros comprehensive HFX spinal cord stimulation (SCS) platform includes a Senza SCS system and support services for the treatment of chronic trunk and limb pain and painful diabetic neuropathy. Senza, Senza II, Senza Omnia, and Senza HFX iQ are the only SCS systems that deliver Nevro's proprietary 10 kHz Therapy. HFX iQ, Nevros latest innovation, is the first and only SCS System that uses Artificial Intelligence to optimize and maintain pain relief using each patient's response1.Nevros unique support services provide every patient with an HFX Coach throughout their pain relief journey and every physician with HFX Cloud insights for enhanced patient and practice management.
Nevro also recently added a minimally invasive treatment option for patients suffering from chronic sacroiliac joint ("SI joint") pain and now provides the most comprehensive portfolio of products in the SI joint fusion space, designed to meet the preferences of physicians and varying patient needs in order to improve outcomes and quality of life for patients.
Job Summary & Responsibilities:The Research Engineer is responsible for investigating and implementing the technical and clinical requirements of the Product Research and Emerging Clinical Indications team. Under the direction of the senior members of the team, the research 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 team.
#LI-JS1
Role Requirements:$134,906 - $168,632. The final starting salary offer to the successful candidate will be determined by evaluating several factors, such as education, experience, knowledge, skills, internal equity, alignment with market data, and geography. *Nevro is a multi-state employer, so the target pay range may increase or decrease depending on the city/state.
Full-time Nevro team members enjoy a full suite of additional benefits such as market-leading medical, dental, and vision benefits, 401k matching, ample vacation time, pre-tax savings perks, tuition reimbursement, Employee Stock Purchase Plan (ESPP), short and/or long-term incentive opportunities, recognition awards, volunteer time off, and several employee resource groups that focus on supporting our Wellness, Leadership Development, and Diversity and Inclusion.
EEO Statement:Nevro offers equal employment opportunity, regardless of race, color, creed, religion, national origin, marital or family status, sex, sexual orientation, gender expression (including religious dress and grooming practices), gender (including pregnancy, childbirth or medical condition related to pregnancy or childbirth), physical or mental condition, protected veteran status, disability, age or other characteristics protected by laws.