Senior Pharmacovigilance Associate

ICON Clinical Research, LP

Sofia, Bulgaria
Hybrid
Adverse event reporting
Safety data analysis
Meddra coding
ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment

Job Summary

  • ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment.
  • As a Senior Pharmacovigilance Associate, you will lead adverse event report management, data analysis, and regulatory document preparation.
  • ICON offers competitive salary, health insurance, retirement planning, employee assistance programs, and flexible country-specific benefits.

Matching Summary

ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment.

Skills & Requirements

Must-have

  • adverse event reporting
  • safety data analysis
  • MedDRA coding
  • pharmacovigilance databases
  • regulatory compliance

Nice-to-have

  • cross-functional collaboration
  • mentorship
  • continuous learning
  • patient safety focus

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Extensive pharmacovigilance experience
  • Proficiency in Argus Safety Database

Work Rights

Not specified

Tailored Resume

Cover Letter