Experienced Clinical Research Associate
IQVIA(2 days ago)
About this role
A Clinical Site Monitor is responsible for overseeing clinical trial sites to ensure compliance with study protocols, regulations, and quality standards. The role involves coordinating site visits, training, documentation, and liaising with study teams to support the successful conduct of clinical research projects.
Required Skills
- GCP
- ICH Guidelines
- Clinical Research
- Site Monitoring
- Regulatory Compliance
- Study Coordination
- Data Management
- Documentation
- Communication
- Problem Solving
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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