Pharmacovigilance Associate

ICON Clinical Research, LP

Mexico City, Mexico
Collecting and analyzing adverse event data
Reporting adverse event information
Regulatory guidelines compliance
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.
  • 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

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 and analyzing adverse event data
  • reporting adverse event information
  • regulatory guidelines compliance
  • signal detection and risk assessment
  • maintaining pharmacovigilance knowledge

Nice-to-have

  • fostering an inclusive environment
  • driving innovation and excellence
  • commitment to patient safety
  • effective collaboration with stakeholders

Key Requirements

  • Bachelor's degree in life sciences, pharmacy, or related field
  • Experience in pharmacovigilance or drug safety
  • Strong analytical skills and attention to detail
  • Excellent communication and interpersonal skills

Work Rights

Not specified

Tailored Resume

Cover Letter