Clinical Research Associate - Sponsor Dedicated
IQVIA(3 months ago)
About this role
This role supports the successful execution of clinical studies by overseeing assigned investigative sites and ensuring study activities align with protocol and sponsor expectations. The position serves as a key point of contact for sites, helping maintain study conduct quality and data integrity throughout the trial lifecycle.
Required Skills
- Site Monitoring
- Clinical Trials
- GCP Compliance
- ICH Guidelines
- Site Management
- Subject Recruitment
- Protocol Training
- Regulatory Submissions
- CRF Review
- Data Queries
+5 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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