Description
We are seeking a Pharmacovigilance Analyst to join our team in Rio de Janeiro, Brazil. As a Pharmacovigilance Analyst, you will execute and support pharmacovigilance activities for GSK Brazil, contributing to patient safety and compliance with regulatory requirements and global standards.
Responsibilities:
- Monitor and control quality of safety-related activities, including individual case management and literature monitoring
- Execute pharmacovigilance activities related to clinical studies and patient assistance programs
- Translate, review, and submit regulatory documents and maintain updated records
- Support notifications, communications, and distribution of safety documents and reports
- Conduct pharmacovigilance training for interface areas and monitor certification completion
- Support risk management and regulatory intelligence activities
Requirements:
- Bachelor's degree in Health Sciences, preferably Pharmacy
- Experience in pharmacovigilance, preferably in post-marketing or clinical studies
- Knowledge of Brazilian regulatory requirements and ANVISA guidelines
- Advanced knowledge of Microsoft Office tools
- Analytical and problem-solving skills, with attention to detail and continuous improvement mindset
Benefits: No specific benefits mentioned.
We offer a dynamic work environment where you can grow and develop your career.
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