Vice President, Medtech Cardiovascular Regulatory Affairs

IQVIA MedTech

Base: $169,200.00 - $471,500.00 annually; bonus/eq...
15+ years regulatory affairs experience
Medical device submission expertise
Team management and mentoring
This role leads the regulatory department, managing strategy, submissions, and client relationships for IQVIA MedTech's cardiovascular portfolio

Job Summary

  • This role leads the regulatory department, managing strategy, submissions, and client relationships for IQVIA MedTech's cardiovascular portfolio.
  • The successful candidate will mentor junior staff, oversee budgets, and drive business development to secure new clients in the medical device sector.
  • Candidates must possess deep domain expertise in FDA and international regulations while demonstrating strong leadership in complex project environments.

Matching Summary

This role leads the regulatory department, managing strategy, submissions, and client relationships for IQVIA MedTech's cardiovascular portfolio.

Salary

Base: $169,200.00 - $471,500.00 annually; Bonus/Equity: Incentive plans may be offered; Benefits: Health, welfare, and other benefits included

Skills & Requirements

Must-have

  • 15+ years regulatory affairs experience
  • Medical device submission expertise
  • Team management and mentoring
  • FDA and international regulatory fluency
  • Project management in life sciences

Nice-to-have

  • Thought leadership in MedTech
  • Business development capabilities
  • Advanced statistical analysis skills
  • Strong technical writing abilities
  • Cross-functional collaboration

Key Requirements

  • Bachelor's degree required; MS or PhD preferred
  • Minimum 15 years in Regulatory Affairs
  • 3-5 years people management experience
  • US and/or International regulatory experience
  • Background in engineering and biology

Work Rights

Not specified

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