Safety Aggregate Report Spec
IQVIA(11 days ago)
About this role
An Associate Scientist in Pharmacovigilance at IQVIA specializes in managing and reviewing safety data, signal detection, and regulatory deliverables related to drug safety. The role involves supporting safety analysis and documentation to ensure compliance with regulatory requirements, working with cross-functional teams, and contributing to safety surveillance activities.
Required Skills
- Microsoft Office
- Signal Management
- Literature Review
- Safety Surveillance
- Regulatory Reporting
- Drug Safety
- Aggregate Reporting
- Medical Terminology
- Data Analysis
- Pharmacovigilance
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
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