FSP Sponsor Dedicated - Study Start-Up Manager
IQVIA(6 days ago)
About this role
This role involves overseeing the delivery of site activation, maintenance, and regulatory activities for clinical studies or multi-protocol programs. It requires providing expert support in regulatory and technical aspects, ensuring compliance with guidelines, and coordinating across regions to support successful clinical trial execution.
Required Skills
- Regulatory Affairs
- Clinical Trials
- GCP
- ICH Guidelines
- Project Management
- Regulatory Strategy
- Contract Negotiation
- Drug Development
- Clinical Documentation
- Quality Assurance
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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