Regulatory Affairs Manager
IQVIA(1 month ago)
About this role
IQVIA is hiring a Regulatory Affairs Manager to serve as a Global Regulatory Lead for human medicinal products. The role focuses on owning the global regulatory roadmap and coordinating worldwide regulatory filings and health authority engagement across major agencies such as EMA and FDA. The position operates within IQVIA’s Regulatory Affairs and Drug Development Solutions organization, leveraging technology-enabled regulatory services to improve approval success and speed to market.
Required Skills
- Regulatory Strategy
- Global Submissions
- EMA Submissions
- FDA Submissions
- Lifecycle Management
- Health Authority Meetings
- Briefing Packages
- Risk Mitigation
- Regulatory Publishing
- RIM Systems
+10 more
Qualifications
- Bachelor’s Degree in Life Sciences
- Master’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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