Pharmacovigilance Assistant

ICON

Warsaw, Poland
Hybrid
Pharmacovigilance data entry
Adverse event report processing
Regulatory safety compliance
As a Pharmacovigilance Assistant I at ICON, you will play a key role in supporting the collection, documentation, and reporting of safety data related to medications and clinical trials

Job Summary

  • As a Pharmacovigilance Assistant I at ICON, you will play a key role in supporting the collection, documentation, and reporting of safety data related to medications and clinical trials.
  • ICON offers a range of benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values and the company is dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

As a Pharmacovigilance Assistant I at ICON, you will play a key role in supporting the collection, documentation, and reporting of safety data related to medications and clinical trials.

Skills & Requirements

Must-have

  • Pharmacovigilance data entry
  • Adverse event report processing
  • Regulatory safety compliance
  • Documentation and record maintenance
  • Cross-functional collaboration
  • Office-based hybrid work

Nice-to-have

  • Attention to detail
  • Organizational skills
  • Effective communication
  • Fast-paced regulated environment
  • Inclusive work culture

Key Requirements

  • Bachelor’s degree in life sciences or pharmacy
  • Basic pharmacovigilance knowledge
  • Ability to work in regulated environment

Work Rights

Not specified

Tailored Resume

Cover Letter