Regulatory and Clinical Trials Lead Job at Subsense Inc., Palo Alto, CA

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  • Subsense Inc.
  • Palo Alto, CA

Job Description

Location: Palo Alto, USA

Position Type: Full-Time

Company Overview:

Subsense is a pioneering organization specializing in developing innovative nanotechnology solutions aimed at revolutionizing the field of noninvasive daily used Brain-Computer Interfaces and treating Neurodegenerative disease. We are committed to creating cutting-edge products that address complex health challenges and improve customer and patient outcomes.

Job Summary:

We're seeking a visionary Regulatory and Clinical Trials Lead to pioneer our journey in brain-computer interface technology. This role offers a unique opportunity to shape the regulatory strategy of a cutting-edge medical device company. You'll be at the forefront of innovation, working with a diverse team to navigate the complex landscape of global medical device regulations. If you're passionate about bringing revolutionary technologies to market, have a knack for building and leading teams, and thrive in a fast-paced startup environment, we want you. Join us in transforming the future of neurotechnology and making a lasting impact on patient care.

Key Responsibilities:

  • Overseeing regulatory department of the company, establishing a regulatory strategy and quality management system in collaboration with external consultants
  • Working with a cross functional, interdisciplinary team to integrate hardware, software, nanoscience, data science, and regulatory to build new BCI technology
  • Collaborating with internal teams and external collaborators to establish medical device clinical trials
  • Interface and negotiate with US and worldwide regulatory agencies
  • Qualify manufacturing partners and suppliers to assure quality standards are maintained
  • Build, grow, and manage the regulatory teams
  • Author regulatory procedures and submissions

Qualifications:

  • Expertise in FDA, EU, and other worldwide medical device regulations
  • Expertise in establishing and maintaining ISO 13485 and FDA compliant QMS systems for high complexity medical devices
  • Experience designing and managing clinical trials for high complexity medical devices
  • Experience with industrial scale up of wearable electronics and medical devices
  • Experience working in early stage startup or other small companies
  • Collaboration experience government agencies and regulatory consultants
  • Management experience leading teams of 4+ people
  • An advanced degree in biomedical engineering, biotechnology or a related field with 6+ years of relevant experience
  • A willingness to take on high risk, high reward challenges
  • Fluent in written and spoken English

What We Offer:

  • Competitive salary and benefits package
  • Opportunity to work in a dynamic and innovative environment
  • Support for professional development and continuous learning
  • Collaborative and inclusive company culture

Job Tags

Full time, Worldwide,

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