CRA 2
IQVIA(1 month ago)
About this role
A Clinical Research Site Monitor at IQVIA supports the execution of clinical trials by ensuring sites adhere to study protocols, regulatory standards, and sponsor requirements. The role helps maintain study documentation and data integrity throughout the study lifecycle. It works with study teams and investigative sites to enable successful trial delivery.
Required Skills
- Site Monitoring
- GCP
- ICH Guidelines
- Recruitment Planning
- Protocol Training
- Regulatory Compliance
- CRF Management
- TMF Management
- Communication
- Microsoft Office
+2 more
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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