Clinical Research Associate, Site Management - Italy
IQVIA(8 months ago)
About this role
Participate in a structured training program to develop the knowledge and skills required to perform clinical monitoring visits. Work under close supervision to support site selection, initiation, monitoring, and close-out activities while ensuring adherence to study protocols and applicable regulatory requirements. The role supports clinical research project execution within IQVIA.
Required Skills
- Clinical Monitoring
- Site Management
- Regulatory Compliance
- GCP
- ICH Guidelines
- Documentation
- Microsoft Office
- Communication Skills
- Enrollment Tracking
- Problem Solving
+1 more
Qualifications
- Bachelor's Degree
- Ministerial Decree (Italy)
- GCP Training
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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