SCRA 1
IQVIA(1 month ago)
About this role
This role focuses on overseeing clinical trial sites to ensure studies are conducted and data are reported according to protocol, regulations, and sponsor requirements. The position serves as the primary point of contact for assigned sites, supporting consistent execution across study phases and maintaining strong site relationships within a global clinical research organization.
Required Skills
- Site Monitoring
- Clinical Trials
- GCP
- ICH
- Site Management
- Study Start-Up
- Subject Recruitment
- Regulatory Submissions
- CRF Review
- Data Queries
+6 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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