(Senior) Clinical Research Associate (CRA)
IQVIA(6 months ago)
About this role
A Clinical Site Monitor supports clinical trials by ensuring sites operate in compliance with study protocols, regulatory requirements, and sponsor expectations to protect participant safety and data integrity. The role sits within a clinical research organization serving life sciences and healthcare clients and involves regular interaction with study sites and study teams.
Required Skills
- Site Monitoring
- Protocol Compliance
- GCP
- ICH
- Recruitment Planning
- Regulatory Submissions
- Documentation
- Data Tracking
- Communication
- Microsoft Office
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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