Pharmacovigilance Specialist

по договоренности
Опыт работы не важен

Job Responsibilities:

  • Performs post surveillance activities such as literature review and media monitoring.
  • Performs reconciliation activities associated with Pharmacovigilance Agreements and various other sources such as product complaints, medical information inquiries.
  • Perform quality check on various sources for ICSR such as Medical Information inquiries, Product Complaints.
  • Assists and supports with documentation management.
  • Support PVA and SDEA processing.
  • Performs and documents contact tests for drug safety to test the mechanisms of reporting to Local Safety Unit.
  • Responsible for keeping relevant databases up to date.
  • Supports the PV-hub team in ensuring high standards are maintained and opportunities for departmental improvements are identified and implemented.
  • Participates in PV project work when necessary and when deemed appropriate
    • Work Environment:

    • Salary - negotiable
    • Social package
      • Requirements:

      • Previous operational experience in Drug Safety/Pharmacovigilance (preferred)
      • Knowledge of Pharmacovigilance regulatory requirements (preferred).
      • Knowledge of medical terminology
      • Ability to evaluate, analyze and interpret data, and draw conclusions, independently
      • Strong organization skills, detail oriented, ability to adapt to change
      • Effective team player, demonstrating initiative and accountability
      • Good communication skills, both written and verbal
      • Identify improvement areas and provide creative problem solving in a complex process-focused environment
      • Ability to work across cultures, including in a virtual environment
      • Computer literate
      • Fluent in English - verbal and written
        • Тип занятости:

          Полная занятость, полный рабочий день, у работодателя

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