Sr. Site Feasibility Specialist
IQVIA(1 month ago)
About this role
This role supports country-level site activation for clinical studies, coordinating startup and maintenance activities to enable investigative sites to become study-ready. It serves as a key liaison between investigative sites and internal teams to keep study initiation moving forward within required guidelines.
Required Skills
- Site Activation
- Study Start-Up
- Regulatory Documents
- Document Tracking
- Clinical Systems
- SOP Compliance
- GCP
- ICH Guidelines
- Ethics Submissions
- Informed Consent
+8 more
Qualifications
- Bachelor’s Degree In Life Sciences Or Related Field
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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