CRA 1
IQVIA(1 month ago)
About this role
This role supports the execution of clinical studies by overseeing trial sites to ensure compliance with study protocols, sponsor requirements, and applicable regulations and guidelines. It involves direct engagement with investigative sites throughout the study lifecycle, with significant travel and ongoing communication to support study delivery and data reliability.
Required Skills
- Clinical Monitoring
- Site Management
- GCP Compliance
- ICH Guidelines
- Site Initiation
- Close-Out Visits
- Subject Recruitment
- Protocol Training
- Regulatory Submissions
- CRF Review
+10 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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