Senior Pharmacovigilance Associate

ICON plc

Sao Paulo, Brazil
Competitive salary; benefits include annual leave,...
Fully remote
Adverse event reporting and processing
Signal detection and data analysis
Periodic safety update reports (psurs)
The role involves leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate regulatory compliance

Job Summary

  • The role involves leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate regulatory compliance.
  • Candidates will collaborate with medical and clinical teams to assess clinical relevance and contribute to risk management activities.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and belonging.

Matching Summary

The role involves leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate regulatory compliance.

Salary

Competitive salary; Benefits include annual leave, health insurance, retirement planning, and global employee assistance program; Flexible country-specific optional benefits available

Skills & Requirements

Must-have

  • Adverse event reporting and processing
  • Signal detection and data analysis
  • Periodic safety update reports (PSURs)
  • Pharmacovigilance database management
  • Regulatory compliance with international guidelines

Nice-to-have

  • Training and mentorship of junior staff
  • Audit and inspection readiness
  • Cross-functional collaboration skills
  • Advanced degree in life sciences
  • Continuous improvement of PV processes

Key Requirements

  • Bachelor's degree in life sciences, pharmacy, or nursing
  • Extensive experience in pharmacovigilance or drug safety
  • Proficiency in pharmacovigilance databases and Microsoft Office
  • Advanced level of English proficiency

Work Rights

Not specified

Tailored Resume

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