Experienced CRA (no travel) - Sponsor Dedicated
IQVIA(1 month ago)
About this role
This role supports a sponsor’s clinical trials by overseeing study sites to ensure protocol compliance and accurate reporting of study data. The position is based in the Netherlands and focuses on maintaining site oversight and coordination to support successful study delivery.
Required Skills
- Site Monitoring
- Clinical Trials
- GCP
- ICH Guidelines
- Site Management
- Subject Recruitment
- Protocol Training
- Regulatory Submissions
- CRF Management
- Data Queries
+7 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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