Pharmacovigilance Administrator

ICON plc

Warsaw, Poland
Hybrid
Administrative coordination
Documentation management
Regulatory requirements
At ICON, you will play a key role behind the scenes of clinical research—ensuring that critical safety information is accurately captured, documented, and reported

Job Summary

  • At ICON, you will play a key role behind the scenes of clinical research—ensuring that critical safety information is accurately captured, documented, and reported.
  • This is a hybrid position, requiring attendance at our Warsaw (Poland) or Sofia (Bulgaria) office three days per week.
  • Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Matching Summary

At ICON, you will play a key role behind the scenes of clinical research—ensuring that critical safety information is accurately captured, documented, and reported.

Skills & Requirements

Must-have

  • administrative coordination
  • documentation management
  • regulatory requirements
  • data entry
  • patient safety information

Nice-to-have

  • structured detail-oriented environments
  • purpose-driven work
  • cross-functional collaboration
  • life sciences background

Key Requirements

  • previous administrative experience
  • experience in regulated environment
  • strong organizational skills
  • high attention to detail
  • experience with data tools

Work Rights

Not specified

Tailored Resume

Cover Letter