Clinical Files Specialist
IQVIA(1 month ago)
About this role
This role provides administrative support to clinical operations teams to ensure accurate, complete Trial Master File (TMF) delivery. It supports coordination across Clinical Research Associates and Regulatory/Start-Up teams to keep clinical documentation and tracking systems current and organized within project timelines.
Required Skills
- Trial Master File
- Document Control
- Clinical Documentation
- Regulatory Compliance
- Site Compliance
- Clinical Trial Supplies
- Tracking Management
- Case Report Forms
- Data Flow
- Microsoft Word
+6 more
Qualifications
- High School Diploma
- GCP
- ICH
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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