Admin assistant for clinical trials - Exclusive for People With Disabilities
IQVIA(21 days ago)
About this role
Administrative support role within clinical research focused on ensuring accurate and complete trial documentation and compliance for clinical studies. The position supports Clinical Research Associates and Regulatory/Start‑Up teams and is offered as a hybrid role based in São Paulo.
Required Skills
- TMF Management
- Document Management
- Filing
- Archiving
- CRF Tracking
- Clinical Data
- Supply Tracking
- Communication
- Excel
- English
Qualifications
- Bachelor's Degree (Life Sciences)
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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