Centralized Monitor- Slovak/Czech Speaker
IQVIA(1 month ago)
About this role
A Clinical Study Monitor at IQVIA supports the execution and quality oversight of assigned clinical studies from initiation through closeout, ensuring adherence to SOPs, ICH-GCP, and applicable regulatory requirements. The role focuses on centralized review of clinical data and operational insight across sites to maintain study integrity and patient safety while collaborating with project teams and stakeholders.
Required Skills
- Clinical Monitoring
- Remote Monitoring
- Data Review
- Risk-Based Monitoring
- Site Management
- Trend Analysis
- Project Management
- Regulatory Compliance
- GCP Knowledge
- SOPs
+6 more
Qualifications
- Bachelor's Degree in Clinical, Life Sciences, Mathematical Sciences or Related Field
- Nursing Qualification (optional)
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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