About this role
The role involves performing site monitoring and management tasks to ensure compliance with study protocols, regulations, and sponsor requirements in clinical research settings. The individual will oversee study site activities, training, and documentation to support successful clinical trials.
Required Skills
- GCP
- ICH Guidelines
- Clinical Research
- Regulatory Compliance
- Site Management
- Monitoring
- CRF
- Documentation
- Communication
- Problem Solving
Qualifications
- Bachelor's Degree in scientific discipline or healthcare
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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