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Key Responsibilities:

  • Independently perform ICSR triage, case processing, and quality control after training.
  • Manage safety cases from multiple sources, ensuring completeness and compliance.
  • Perform SAE reconciliation and track outstanding items.

Requirements:

  • Bachelor’s degree in life sciences or healthcare discipline.
  • At least 2 years of experience in drug safety or pharmacovigilance.
  • Working knowledge of global regulatory requirements (ICH, GVP, FDA).

What We Offer:

  • Fully remote position based in Brazil.
  • Opportunity to work on international ICSR activities.
  • Professional development through training and process improvement.

Partner Company

This company is a partner organization focused on global pharmacovigilance operations. It is a fast-growing, internationally focused company with a collaborative culture emphasizing teamwork, excellence, and continuous improvement.

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