Experienced Clinical Research Associate
IQVIA(4 months ago)
About this role
This role supports the delivery of clinical studies by overseeing study sites to ensure they meet protocol requirements, sponsor expectations, and regulatory guidelines. It focuses on maintaining oversight of site performance and study documentation while serving as a key point of coordination between sites and the broader study team.
Required Skills
- Site Monitoring
- Clinical Trials
- Site Management
- GCP Compliance
- ICH Guidelines
- Subject Recruitment
- Protocol Training
- Regulatory Submissions
- CRF Management
- Data Queries
+7 more
Qualifications
- High School Diploma
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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