Clinical Research Associate 1/2
IQVIA(2 months ago)
About this role
This role supports clinical trials by overseeing study sites to ensure protocol compliance and accurate reporting in line with regulatory standards and sponsor expectations. The position involves direct interaction with investigative sites to maintain study progress and documentation throughout the trial lifecycle.
Required Skills
- Clinical Monitoring
- Site Management
- GCP
- ICH
- Site Initiation
- Close-Out Visits
- Subject Recruitment
- Site 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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