Senior Pharmacovigilance Associate

ICON plc

Warsaw, Poland
Adverse event reporting
Safety data analysis
Regulatory document preparation
ICON plc is a world-leading healthcare intelligence and clinical research organization seeking to shape the future of clinical development

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization seeking to shape the future of clinical development.
  • As a Senior Pharmacovigilance Associate, you will lead adverse event reporting, data analysis, and regulatory submissions to ensure patient safety.
  • ICON offers competitive salary, a range of benefits focused on well-being and work-life balance, and fosters an inclusive and diverse culture.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking to shape the future of clinical development.

Skills & Requirements

Must-have

  • adverse event reporting
  • safety data analysis
  • regulatory document preparation
  • pharmacovigilance databases
  • cross-functional team collaboration

Nice-to-have

  • mentorship of junior team members
  • audit and inspection readiness
  • inclusive and diverse culture
  • commitment to confidentiality

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Extensive experience in pharmacovigilance or drug safety
  • Proven ability to manage pharmacovigilance process
  • Strong analytical and critical thinking skills
  • Proficiency in pharmacovigilance databases
  • Ability to work independently

Work Rights

Not specified

Tailored Resume

Cover Letter