Regulatory Affairs Scientist

Dexcom Corporation

$71,600.00 - $119,300.00 py
Leveraging data analytics for regulatory strategy
Support global advertising and promotional efforts
Monitor competitive landscape and regulatory trends
The Regulatory Scientist will work within Regulatory Affairs, Government Affairs and Global Advocacy and collaborate with cross-functional teams to support efforts for Dexcom’s digital health, software-enabled products, Ad/Promo activities, and advocacy and policy analysis efforts

Job Summary

  • The Regulatory Scientist will work within Regulatory Affairs, Government Affairs and Global Advocacy and collaborate with cross-functional teams to support efforts for Dexcom’s digital health, software-enabled products, Ad/Promo activities, and advocacy and policy analysis efforts.
  • You develop dashboards and visualizations to communicate metrics and trends across geographies and products.
  • You have experience with medical device development and regulatory processes, especially for software as a medical device (SaMD).

Matching Summary

The Regulatory Scientist will work within Regulatory Affairs, Government Affairs and Global Advocacy and collaborate with cross-functional teams to support efforts for Dexcom’s digital health, software-enabled products, Ad/Promo activities, and advocacy and policy analysis efforts.

Salary

$71,600.00 - $119,300.00

Skills & Requirements

Must-have

  • Leveraging data analytics for regulatory strategy
  • Support global advertising and promotional efforts
  • Monitor competitive landscape and regulatory trends
  • Lead discussions on new technologies
  • Develop engaging narratives around technical information
  • Establish cross-functional relationships for evidence generation

Nice-to-have

  • Passionate about digital health and AI/ML
  • Familiar with evolving digital health policy
  • Agile software development experience
  • Warrior-like ambition and passion

Key Requirements

  • Bachelor's degree and 2-5 years of related experience
  • Experience with medical device development and regulatory processes
  • Experience with Software as a Medical Device (SaMD)
  • Strong analytical skills
  • Proficiency in visualization platforms (Tableau or Power BI)
  • Familiarity with regulatory data sources and standards

Work Rights

Not specified

Tailored Resume

Cover Letter