Senior Clinical Regulatory Scientist

VB Spine

Leesburg, VA, United States
Base: $85,000 - $110,000 annually; bonus/equity: p...
Hybrid (20% travel required)
Clinical evaluation plans and reports
Systematic literature reviews
Regulatory-compliant clinical evidence
VB Spine is seeking a Senior Clinical Regulatory Scientist for its Leesburg, VA location, where the candidate will play a key role in developing regulatory-compliant clinical evidence documentation for spinal medical devices. The company emphasizes innovation and collaboration within a mission-driven culture focused on improving patient outcomes

Job Summary

  • At VB Spine, you’ll be part of a mission-focused team that supports surgeons during life-changing spinal procedures.
  • As a Senior Clinical Regulatory Scientist, you will translate complex scientific data into clear, submission-ready materials that support global product registrations and ongoing device safety.
  • The company offers competitive pay, comprehensive benefits, ongoing professional development, and opportunities for growth within a fast-paced, dynamic environment.

Matching Summary

Match Score: 85

VB Spine is seeking a Senior Clinical Regulatory Scientist for its Leesburg, VA location, where the candidate will play a key role in developing regulatory-compliant clinical evidence documentation for spinal medical devices. The company emphasizes innovation and collaboration within a mission-driven culture focused on improving patient outcomes.

Salary

Base: $85,000 - $110,000 annually; Bonus/Equity: Potential for bonuses and incentives; Benefits: Comprehensive health, dental, vision insurance, 401(k) with match, PTO, training

Skills & Requirements

Must-have

  • Clinical Evaluation Plans and Reports
  • Systematic literature reviews
  • Regulatory-compliant clinical evidence
  • Cross-functional collaboration
  • Medical device regulatory knowledge
  • Scientific and medical writing skills

Nice-to-have

  • Process-oriented mindset
  • Independent judgment and communication
  • Experience with literature management software
  • Ability to manage complex projects
  • Collaboration with external stakeholders

Key Requirements

  • Bachelor’s degree in technical or scientific discipline
  • Master’s, Ph.D., or advanced health-related degree preferred
  • Minimum 1+ year scientific or medical writing experience
  • 2+ years clinical, medical, quality, or regulatory affairs experience preferred
  • Knowledge of global clinical regulatory requirements
  • Ability to travel up to 20%

Work Rights

Not specified

Tailored Resume

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