Pharmacovigilance Associate

ICON Clinical Research, LP

Sao Paulo, Brazil
Collecting adverse event reports
Analyzing adverse event data
Reporting adverse event information
As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information

Job Summary

  • As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.
  • Your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.

Skills & Requirements

Must-have

  • collecting adverse event reports
  • analyzing adverse event data
  • reporting adverse event information
  • regulatory guidelines compliance
  • signal detection activities
  • risk assessment activities

Nice-to-have

  • fostering an inclusive environment
  • driving innovation and excellence
  • commitment to patient safety
  • maintaining high standards of quality

Key Requirements

  • Bachelor's degree in life sciences, pharmacy, or related field
  • Experience in pharmacovigilance or drug safety
  • Experience in a clinical or pharmaceutical environment
  • Strong analytical skills
  • Excellent communication and interpersonal skills

Work Rights

Not specified

Tailored Resume

Cover Letter