CRA2
IQVIA(1 month ago)
About this role
A Clinical Research Associate at IQVIA supports the conduct and oversight of clinical trials to ensure studies meet protocol, regulatory, and sponsor standards. The role focuses on maintaining data integrity and regulatory adherence while facilitating communication between study sites and the sponsor. It contributes to the overall execution and quality of clinical research programs.
Required Skills
- Site Monitoring
- GCP
- ICH Guidelines
- Patient Recruitment
- Regulatory Compliance
- TMF Management
- CRF Management
- Documentation
- Communication
- Time Management
+1 more
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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