Pharmacovigilance Regulatory Reporting Specialist
Remote · São Paulo, São Paulo, Brazil or Buenos Aires, Buenos Aires F.D., Argentina
Job Summary
Regulatory Reporting Specialist in pharmacovigilance responsible for submitting safety reports to regulatory authorities, reviewing and processing safety data, and distributing reports to internal/external parties in accordance with regulations, SOPs, and project guidelines. Collaborates with health care professionals and cross-functional teams; tracks cases; identifies quality issues; and supports project delivery under senior guidance. Extensive use of safety databases and Argus, with focus on accuracy, compliance, and timely communication. 100% home-based position with IQVIA, requiring professional communication and teamwork across multiple regional sites.
Required Qualifications
- Bachelor's degree in life sciences
- 2-3 years of pharmacovigilance experience
- Experience with regulatory reporting
- Proficiency with Argus
- Good knowledge of medical terminology and safety databases
- Strong organizational skills and attention to detail
- Ability to work independently and in a team
- Advanced level of English
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