CRA 1 - Brazil
IQVIA(1 month ago)
About this role
This role supports clinical research studies in Brazil by overseeing study sites to ensure compliance with protocols, regulations, and sponsor expectations. The position focuses on maintaining strong site relationships, ensuring data and documentation integrity, and helping studies progress smoothly from start-up through close-out. It is part of IQVIA’s clinical research services supporting life sciences and healthcare clients.
Required Skills
- Site Monitoring
- Clinical Trials
- GCP Compliance
- ICH Guidelines
- Site Management
- Subject Recruitment
- Protocol Training
- Regulatory Submissions
- CRF Management
- Data Queries
+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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