Clinical Research Coordinator, On-Site, Pleasant View, UT
IQVIA(7 days ago)
About this role
This role involves supporting clinical research activities, including data collection, patient interaction, procedure execution, and compliance with regulatory standards. It emphasizes coordination, documentation, and communication within clinical trial settings to ensure study objectives are met.
Required Skills
- clinical Procedures
- Regulatory Compliance
- Data Collection
- Patient Interaction
- Laboratory Skills
- Protocol Review
- Study Coordination
- Medical Assistance
- Spirometry
- ECG
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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