Pharmacovigilance Specialist

4 semanas atrás


Lisboa, Lisboa, Portugal Organon Tempo inteiro

Job Summary

We are seeking a highly skilled Pharmacovigilance Specialist to join our team. The ideal candidate will have a strong background in pharmacovigilance and regulatory affairs, with a minimum of 1 year of industry experience.

Key Responsibilities

  • Manage day-to-day adverse events case intake and follow-up activities in accordance with Global Pharmacovigilance procedures and country regulations.
  • Track and translate Individual Case Safety Reports (ICSRs) from designated points of contact, vendors, and business partners.
  • Execute local PV processes and activities in alignment with PV systems and their associated Quality Management System.
  • Perform reconciliation activities for PV cases received from local operating units and contractual partners.

Requirements

  • Bachelor’s degree in health, life science, or medical science.
  • Fluent in English and proficient in local language.
  • Proven experience in pharmacovigilance and regulatory affairs.

About Us

Organon is a leading healthcare company dedicated to improving people’s lives through innovative pharmaceuticals and solutions. We are committed to advancing medical science, improving patient outcomes, and enhancing the quality of life for people around the world.


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