Clinical Research Associate Sponsor-dedicated
IQVIA(2 months ago)
About this role
This role supports the successful execution of clinical studies by overseeing site performance and ensuring study data is collected and reported according to protocol and sponsor requirements. The position serves as a key point of contact between study sites and the project team to maintain study progress and documentation quality. It operates within a regulated clinical research environment focused on patient safety and data integrity.
Required Skills
- Site Monitoring
- Study Start-Up
- GCP
- ICH
- Site Management
- Subject Recruitment
- Protocol Training
- Regulatory Submissions
- CRF Review
- Data Queries
+8 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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