Regulatory Affairs Specialist
IQVIA(1 month ago)
About this role
A Regulatory Affairs Specialist at IQVIA supports compliance and product lifecycle management for medicinal products across Germany, Switzerland, and Austria, working with global pharmaceutical clients. The role contributes to high-quality regulatory outcomes that advance healthcare and patient access to medicines.
Required Skills
- Regulatory Submissions
- Labeling Translation
- Document Preparation
- Stakeholder Management
- Legislation Knowledge
- MS Office
- Artwork Review
- Project Coordination
- Communication
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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