Pharmacovigilance Supervisor

ICON

Sao Paulo, Brazil
Pharmacovigilance operations supervision
Adverse event safety reporting
Global regulatory compliance
As a Supervisor, Pharmacovigilance at ICON, you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products

Job Summary

  • As a Supervisor, Pharmacovigilance at ICON, you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products.
  • ICON offers a range of benefits designed to support well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
  • ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.

Matching Summary

As a Supervisor, Pharmacovigilance at ICON, you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products.

Skills & Requirements

Must-have

  • Pharmacovigilance operations supervision
  • Adverse event safety reporting
  • Global regulatory compliance
  • Safety data collection and analysis
  • Team leadership and training

Nice-to-have

  • Cross-functional collaboration
  • Detail-oriented multitasking
  • Inclusive and diverse work culture

Key Requirements

  • Bachelor’s degree in life sciences or pharmacy
  • Experience in pharmacovigilance or drug safety
  • Knowledge of global pharmacovigilance regulations

Work Rights

Not specified

Tailored Resume

Cover Letter