Senior Pharmacovigilance Associate

ICON Clinical Research, LP

Mexico City, Mexico
Adverse event reporting
Signal detection
Pharmacovigilance databases
ICON is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development

Job Summary

  • ICON is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development.
  • As a Senior Pharmacovigilance Associate, you will lead the collection, evaluation, and processing of adverse event reports and conduct data analysis to identify safety signals.
  • ICON offers competitive salary, diverse benefits focused on well-being and work-life balance, and fosters an inclusive and accessible environment.

Matching Summary

ICON is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development.

Skills & Requirements

Must-have

  • adverse event reporting
  • signal detection
  • pharmacovigilance databases
  • regulatory compliance
  • data analysis and interpretation

Nice-to-have

  • mentorship of junior team members
  • audit and inspection readiness
  • fostering an inclusive environment
  • commitment to confidentiality

Key Requirements

  • Bachelor's degree in life sciences, pharmacy, nursing, or related field
  • Extensive experience in pharmacovigilance or drug safety
  • Proficiency in pharmacovigilance databases and Microsoft Office Suite
  • Ability to work independently and manage multiple priorities

Work Rights

Not specified

Tailored Resume

Cover Letter