2026 CRA ADP Beijing Shanghai
IQVIA(1 month ago)
About this role
This role is part of a structured training program focused on developing the knowledge and capabilities to independently conduct clinical trial monitoring visits. The position supports clinical research activities at investigational sites while learning IQVIA processes and industry standards within a global life sciences services organization.
Required Skills
- Clinical Monitoring
- Site Visits
- GCP
- ICH Guidelines
- Clinical Research
- Site Training
- Regulatory Submissions
- TMF
- ISF
- CRF Management
+8 more
Qualifications
- Bachelor's Degree
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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