Site Research Assistant - Kansas City, MO
IQVIA(2 months ago)
About this role
IQVIA is hiring an on-site Research Assistant to support clinical trial operations while ensuring compliance with applicable regulations. The role supports study teams by helping with participant coordination and maintaining essential study documentation in a clinical research environment.
Required Skills
- EDC Entry
- Query Resolution
- Regulatory Documentation
- Visit Scheduling
- Subject Recruitment
- Subject Screening
- Informed Consent
- IRB Compliance
- GCP Compliance
- Clinical Trial Support
+4 more
Qualifications
- Associate’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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