CRA2
IQVIA(1 month ago)
About this role
A Clinical Research Associate at IQVIA supports the conduct and integrity of clinical studies across investigational sites, ensuring studies meet protocol, regulatory, and sponsor expectations. The role contributes to overall trial execution, documentation quality, and communication between sites and study teams.
Required Skills
- Site Monitoring
- GCP
- ICH Guidelines
- Protocol Knowledge
- CRF Management
- Recruitment Planning
- Regulatory Submissions
- Source Documentation
- Microsoft Office
- Communication
Qualifications
- High School Diploma
- Degree In Scientific Discipline (Preferred)
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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