Regulatory Affairs Specialist
IQVIA(1 month ago)
About this role
The Regulatory Affairs Specialist at IQVIA supports product lifecycle management and compliance for medicinal products across Germany, Switzerland, and Austria. The role partners with global pharmaceutical clients to deliver high-quality regulatory outcomes and contribute to improved patient access to therapies.
Required Skills
- Regulatory Submissions
- Product Labeling
- German Language
- Artwork Review
- Regulatory Maintenance
- Legislation Monitoring
- Project Coordination
- Communication
- MS Office
- Regulatory Systems
Qualifications
- Bachelor's Degree in Life Sciences
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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