Sr CRA1
IQVIA(1 month ago)
About this role
This role focuses on overseeing clinical trial sites to ensure studies are conducted and data are reported in line with the protocol, sponsor requirements, and applicable regulations. The position involves direct engagement with research sites across the study lifecycle, supporting consistent execution and study progress. It is based in Mexico City with significant travel.
Required Skills
- Site Monitoring
- Clinical Trials
- GCP Compliance
- ICH Guidelines
- Site Management
- Study Start-Up
- Regulatory Submissions
- Patient Recruitment
- CRF Management
- TMF Filing
+5 more
Qualifications
- Bachelor'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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