Site Research Assistant - Naples, FL
IQVIA(1 month ago)
About this role
A Research Assistant supporting clinical trial operations to ensure adherence to regulatory, ethical, and organizational standards. The role focuses on maintaining data accuracy, participant safety, and smooth study execution while working on-site part-time.
Required Skills
- EDC
- Data Entry
- Regulatory Binder
- Visit Scheduling
- Recruitment
- Medical History
- Lab Coordination
- Informed Consent
- GCP
- Query Management
+1 more
Qualifications
- Associate 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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