Pharmacovigilance Associate / Senior Associate

ICON plc

Mexico City, Mexico
Competitive salary; benefits: various annual leave...
Hybrid
Leading pv studies or projects
Extensive pharmacovigilance experience
Adverse event reporting management
ICON plc is seeking a Senior Pharmacovigilance Associate in Mexico City to oversee pharmacovigilance activities, ensuring the safety and efficacy of pharmaceutical products. The ideal candidate will have extensive experience in drug safety, strong analytical skills, and the ability to collaborate with cross-functional teams

Job Summary

  • The role involves leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate regulatory reporting.
  • ICON offers a competitive salary along with comprehensive benefits including health insurance, retirement planning, and global employee assistance programs.
  • Candidates must have a Bachelor's degree in life sciences or pharmacy and proven experience in managing pharmacovigilance processes.

Matching Summary

Match Score: 85

ICON plc is seeking a Senior Pharmacovigilance Associate in Mexico City to oversee pharmacovigilance activities, ensuring the safety and efficacy of pharmaceutical products. The ideal candidate will have extensive experience in drug safety, strong analytical skills, and the ability to collaborate with cross-functional teams.

Salary

Competitive salary; Benefits: Various annual leave, health insurance, retirement planning, TELUS Health; Flexible country-specific optional benefits

Skills & Requirements

Must-have

  • Leading PV studies or projects
  • Extensive pharmacovigilance experience
  • Adverse event reporting management
  • Signal detection and analysis
  • Regulatory compliance knowledge

Nice-to-have

  • Strong analytical and critical thinking
  • Mentoring junior team members
  • Cross-functional collaboration skills
  • Proficiency in PV databases
  • Commitment to patient safety

Key Requirements

  • Bachelor's degree in life sciences, pharmacy, nursing
  • Experience in leading PV studies or projects
  • Extensive experience in pharmacovigilance or drug safety
  • CVs and assessments submitted in English

Work Rights

Not specified

Tailored Resume

Cover Letter