Reg Affairs Officer 2, IQVIA Biotech
IQVIA(25 days ago)
About this role
Senior regulatory professional at IQVIA supporting life sciences and pharmaceutical clients. An individual contributor with deep subject-matter knowledge in regulatory affairs, particularly Chemistry, Manufacturing and Controls (CMC), lifecycle maintenance, and marketing authorizations. Works under limited supervision and provides expert input to projects across clinical research and commercialization.
Required Skills
- Regulatory Leadership
- Technical Writing
- Documentation
- Client Relations
- CMC
- Lifecycle Management
- Labeling
- Publishing
- Budget Management
- Training
+2 more
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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