Study Site Management Specialist - Germany - Home Based (m/w/d)
IQVIA(13 days ago)
About this role
A Site Activation Specialist at IQVIA supports the process of initiating clinical trial sites, ensuring regulatory compliance and quality standards are met at a country level. The role involves coordinating documentation, liaising with sites and internal teams, and managing timelines for study startup activities. It requires local expertise, language fluency, and experience in clinical research operations.
Required Skills
- Regulatory Compliance
- Clinical Research
- Documentation
- Quality Control
- Project Management
- GCP/ICH
- Site Management
- Regulatory Submissions
- Data Tracking
- Communication
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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