Senior Pharmacovigilance Associate

ICON

Mexico City, Mexico
Adverse event reporting management
Pharmacovigilance database proficiency
Regulatory compliance in pharmacovigilance
As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and efficacy of pharmaceutical products by managing and overseeing pharmacovigilance activities

Job Summary

  • As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and efficacy of pharmaceutical products by managing and overseeing pharmacovigilance activities.
  • ICON offers a diverse and inclusive culture that rewards high performance and nurtures talent, with competitive salary and a range of benefits focused on well-being and work-life balance.
  • The role involves leading adverse event reporting, preparing regulatory safety reports, collaborating with clinical teams, and ensuring compliance with evolving regulatory guidelines.

Matching Summary

As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and efficacy of pharmaceutical products by managing and overseeing pharmacovigilance activities.

Skills & Requirements

Must-have

  • Adverse event reporting management
  • Pharmacovigilance database proficiency
  • Regulatory compliance in pharmacovigilance
  • Safety data analysis and interpretation
  • Risk management collaboration

Nice-to-have

  • Training and mentoring junior staff
  • Cross-functional team collaboration
  • Handling sensitive patient information
  • Strong communication and interpersonal skills

Key Requirements

  • Bachelor’s degree in life sciences or related field
  • Extensive pharmacovigilance or drug safety experience
  • Strong understanding of pharmacovigilance regulations
  • Ability to manage pharmacovigilance processes
  • Proficiency in Microsoft Office Suite

Work Rights

Not specified

Tailored Resume

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