Nevro Corp.

Senior Clinical Research Scientist

US-CA-Redwood City
2 weeks ago
ID
2017-1953
Category
Clinical

About Nevro

Nevro is a medical device company headquartered in Redwood City, California. We have developed HF10™ therapy, an innovative, evidence-based neuromodulation platform for the treatment of 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 advanced the state of spinal cord stimulation (SCS).

The Nevro® Senza® SCS System received CE mark in 2010, TGA approval in 2011, FDA approval in 2015, and is commercially available in Europe, Australia, and the United.

Overview

This position will be responsible for defining research strategies, goals, and objectives and implementing them, using internal and external resources. Focus on developing and running clinical research for Nevro therapy, analyzing and disseminating the generated evidence.

Role Requirements

  • M.S. or Ph.D. Degree in science/health/engineering (e.g., Neuroscience, and/or Biomedical Engineering) preferred.
  • 5+ years’ experience in clinical/scientific research, medical devices/pharmaceutical clinical trials, plus 2+ years’ experience in medical writing.

 

Skills and Knowledge

  • Develop and run sponsored clinical studies and assist with investigator-initiated studies
  • Develop and review protocols, informed consent, investigator’s brochure for projects
  • Engage and collaborate with US physicians/clinicians on design and implementation of feasibility & new indication clinical studies
  • Organize and analyze data from clinical research to build new hypothesis
  • Communicate/educate as company expert for Nevro clinical science
  • Provide scientific evidence to support strategic decision making for R&D, marketing, clinical, and business development departments
  • Assist in development and preparation of abstracts, posters, manuscripts, literature search and present scientific findings and activities at conferences
  • Assist in planning for, and participate in investigator and coordinator meetings, representing the therapeutic area or region
  • Participate in the dissemination of clinical information to the clinical team members and extended core team members, as appropriate
  • Collaborate and educate clinical project/program managers and clinical operations staff
  • May require up to 20% of travel within continental United States
  • Work with minimal supervision and a self-starter

 

#LI-GR1

 

Options

Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed

Connect With Us!

Not ready to apply? Connect with us for general consideration.