Clinical Research Associate, Full Service
IQVIA(29 days ago)
About this role
A Clinical Research Associate at IQVIA oversees monitoring and site management activities to ensure clinical studies are conducted and reported in compliance with study protocols, regulations, and sponsor requirements. The role supports trial execution by maintaining regulatory documentation, liaising with study teams, and helping to ensure data integrity and subject recruitment performance.
Required Skills
- Site Monitoring
- Site Management
- Subject Recruitment
- Protocol Training
- Quality Assurance
- Regulatory Compliance
- TMF Management
- Documentation
- Communication
- Time Management
+2 more
Qualifications
- Bachelor's Degree
- CRA Training Program
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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