Centralized Monitoring Asst
IQVIA(26 days ago)
About this role
A Clinical Study Support Specialist at IQVIA provides project-related administrative and data support to clinical study management teams, ensuring work aligns with SOPs, Good Clinical Practice, and regulatory requirements. The role supports study tracking, reporting, access management, and central monitoring activities to help identify and mitigate site-level risks.
Required Skills
- Administrative Support
- Data Entry
- Excel
- Reporting
- Systems Management
- Access Management
- Risk Identification
- Site Monitoring
- GCP Knowledge
- Communication
+1 more
Qualifications
- Graduate/Postgraduate in 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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