Sr. Principal, Patient Safety & Experience

Alcon

Fort Worth, Texas, United States
Review adverse event cases
Assess clinical significance of safety data
Ensure regulatory compliance fda eu mdr
This role is responsible for evaluating safety signals from clinical trials and post-market surveillance data to ensure patient safety

Job Summary

  • This role is responsible for evaluating safety signals from clinical trials and post-market surveillance data to ensure patient safety.
  • The position requires ensuring compliance with regulatory standards such as US FDA and EU MDR while communicating findings to stakeholders.
  • Alcon offers a robust benefits package including health, life, retirement, and flexible time off for successful candidates.

Matching Summary

This role is responsible for evaluating safety signals from clinical trials and post-market surveillance data to ensure patient safety.

Skills & Requirements

Must-have

  • Review adverse event cases
  • Assess clinical significance of safety data
  • Ensure regulatory compliance FDA EU MDR
  • Prepare periodic safety updates
  • Conduct signal triage activities

Nice-to-have

  • Collaborate with internal teams
  • Support health authority inquiries
  • Maintain detailed safety records
  • Present findings to safety boards

Key Requirements

  • 7 years of relevant experience preferred
  • Bachelor's degree or equivalent experience
  • M.D. Ophthalmologist or O.D. preferred
  • Fluent English communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter