Clinical Trial Assistant
IQVIA(1 month ago)
About this role
This role provides administrative and coordination support to clinical research teams at IQVIA, helping keep study documentation and communication organized across clinical trials. The position supports site and study operations by maintaining key trial records and assisting with clinical supply and data flow tracking. It is based within a global clinical research services organization supporting the life sciences and healthcare industries.
Required Skills
- Trial Master File
- Document Control
- Clinical Documentation
- Site Compliance
- Clinical Trial Supplies
- Case Report Forms
- Query Tracking
- Data Management
- Clinical Communications
- Microsoft Word
+7 more
Qualifications
- High School Diploma
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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