
Safety Data Analyst with Pharmaceutical Expertise
Há 4 dias
Review, assess, and process safety data and information across service lines. This involves receiving data from various sources, distributing reports to both internal and external third parties following applicable regulations and guidelines.
- Process safety data according to applicable regulations and guidelines.
- Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs), determining the status of events, database entry, coding AEs and products, writing narratives, and literature-related activities.
- Ensure compliance with quality, productivity, and delivery standards.
- Liaise with functional team members and healthcare professionals to address project-related issues.
Qualifications:
- Bachelor's degree in life sciences or a related field.
- Advanced level of English and Portuguese.
- 1+ year of previous experience in clinical research.
IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence. We create connections to accelerate medical treatment development and commercialization.
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