Site Research Assistant - Southfield, MI
IQVIA(1 month ago)
About this role
A Research Assistant at IQVIA supports on-site clinical trial activities, ensuring study operations align with applicable regulations and documentation standards. The role focuses on coordinating study-related tasks and communication with the study team, investigators, and participants in a clinical research environment.
Required Skills
- EDC Entry
- Query Resolution
- Regulatory Documentation
- Visit Scheduling
- Subject Recruitment
- Subject Enrollment
- Informed Consent
- IRB Compliance
- GCP Compliance
- Clinical Trial Support
+3 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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