Site Research Assistant - Merrillville, IN
IQVIA(4 days ago)
About this role
The Site Research Assistant supports clinical trial activities, including data entry, patient chart review, scheduling, and regulatory compliance. The role is vital for ensuring the smooth operation of cardiovascular studies and maintaining regulatory standards.
Required Skills
- EDC
- Clinical Trials
- GCP
- Patient Scheduling
- Regulatory Compliance
- Data Entry
- Chart Review
- Vital Signs
- Laboratory Coordination
- Study Documentation
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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