Especialista Asociado De Farmacovigilancia (fv)- Cono Sur

539

Hybrid
Fluent english oral and written skills
Adverse event case management
Regulatory compliance knowledge
The job posting is for an Associate Specialist in Pharmacovigilance for Cono Sur, responsible for ensuring compliance with regulatory standards and managing adverse event reports. The ideal candidate should have a background in health sciences, experience in the pharmaceutical industry, and fluency in both English and the local language

Job Summary

  • The specialist is responsible for executing local pharmacovigilance activities under supervision to ensure compliance with applicable regulations.
  • Key duties include managing adverse event cases, performing translations between English and Spanish, and submitting reports to regulatory authorities.
  • The role requires supporting audits, implementing corrective actions, and monitoring health authority websites for safety alerts.

Matching Summary

Match Score: 85

The job posting is for an Associate Specialist in Pharmacovigilance for Cono Sur, responsible for ensuring compliance with regulatory standards and managing adverse event reports. The ideal candidate should have a background in health sciences, experience in the pharmaceutical industry, and fluency in both English and the local language.

Skills & Requirements

Must-have

  • Fluent English oral and written skills
  • Adverse event case management
  • Regulatory compliance knowledge
  • Spanish language proficiency
  • Office software proficiency

Nice-to-have

  • Detail-oriented approach
  • Strong communication skills
  • Time management abilities
  • Experience in pharmaceutical industry
  • Data quality assurance skills

Key Requirements

  • Degree in health sciences or equivalent experience
  • Fluent English required (exclusionary)
  • Intermediate to professional Office skills
  • Knowledge of adverse event reporting requirements

Work Rights

Not specified

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