Senior/Clinical Research Associate(Beijing/Shanghai/Guangzhou/Other Cities)
IQVIA(1 month ago)
About this role
This role supports clinical research studies by overseeing and managing trial sites to ensure study conduct and data reporting align with protocol requirements and sponsor expectations. The position works closely with investigative sites and internal study teams to support smooth study execution and predictable enrollment progress. It operates within a regulated clinical research environment.
Required Skills
- Clinical Monitoring
- Site Management
- GCP Compliance
- ICH Guidelines
- Site Initiation
- Close-Out Visits
- Patient Recruitment
- Protocol Training
- Regulatory Submissions
- CRF Review
+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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