CRA 2 - Brazil
IQVIA(3 months ago)
About this role
This role supports the oversight of clinical research study sites to ensure trial activities and data reporting align with the study protocol and sponsor expectations. The position partners closely with investigative sites and internal study teams to keep studies progressing smoothly and in compliance with applicable guidelines. It is based in São Paulo, Brazil, within a global clinical research services organization.
Required Skills
- Site Monitoring
- Clinical Trials
- GCP Compliance
- ICH Guidelines
- Site Management
- Subject Recruitment
- Study Training
- Regulatory Submissions
- Enrollment Tracking
- CRF Review
+6 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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