Post-market Clinical Affairs Specialist

Solventum

Remote, United States
Base: $106,000 - $145,750; bonus/equity: variable ...
Fully remote
Eu mdr regulatory compliance
Post-market clinical follow-up activities
Real world evidence concepts
Solventum is seeking a Post-market Clinical Affairs Specialist to ensure regulatory compliance and support post-market clinical activities in the medical device industry. The role requires a strong background in regulatory requirements and clinical evaluation, particularly in the dental sector, and offers competitive compensation and benefits in a fully remote setting

Job Summary

  • The role involves ensuring regulatory compliance across the product lifecycle by leading Post-Market Clinical Follow-Up activities in alignment with EU MDR and global requirements.
  • Candidates will support cross-functional partners to interpret post-market clinical activities and ensure the safe and effective use of dental products.
  • Solventum offers competitive pay ranging from $106,000 to $145,750 along with a comprehensive benefits package including health, dental, vision, and retirement plans.

Matching Summary

Match Score: 85

Solventum is seeking a Post-market Clinical Affairs Specialist to ensure regulatory compliance and support post-market clinical activities in the medical device industry. The role requires a strong background in regulatory requirements and clinical evaluation, particularly in the dental sector, and offers competitive compensation and benefits in a fully remote setting.

Salary

Base: $106,000 - $145,750; Bonus/Equity: Variable incentive pay eligible; Benefits: Medical, Dental, Vision, HSA, FSA, Disability, Life Insurance, Paid Absences, Retirement

Skills & Requirements

Must-have

  • EU MDR regulatory compliance
  • Post-Market Clinical Follow-Up activities
  • Real World Evidence concepts
  • Clinical evaluation documentation
  • Risk management frameworks

Nice-to-have

  • Dental device industry experience
  • Cross-cultural team collaboration
  • Strategic critical thinking skills
  • Strong medical writing abilities

Key Requirements

  • Bachelor's degree in scientific discipline
  • 3 years medical device industry experience
  • 3 years PMCF and clinical evaluation experience
  • Legal authorization to work in US without sponsorship

Work Rights

Must be legally authorized to work in country without sponsorship

Tailored Resume

Cover Letter