Regulatory and Start up Manager
IQVIA(2 months ago)
About this role
This role coordinates the operational and strategic aspects of clinical trial regulatory submissions, guiding submissions from initial strategy through clinical trial approval. It supports cross-functional stakeholders and ensures submissions are properly prepared and managed within relevant submission systems at IQVIA.
Required Skills
- Clinical Trial Submissions
- Submission Strategy
- CTIS
- Quality Checks
- Regulatory Submissions
- Stakeholder Management
- Project Management
- Financial Planning
- Budget Tracking
- Clinical Research
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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