IQVIA Hiring Centralized Site Associate
Job Overview
Position: Centralized Site Associate
Organization: IQVIA
Location: Mumbai & Bengaluru
Experience: 2 – 5 Years
Qualification: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences
Application Mode: Online Application
Deadline: February 14, 2025
Key Responsibilities
- Provide administrative support to clinical study management teams.
- Perform centralized monitoring to assess site quality and compliance.
- Prepare i-site packs and ensure data accuracy.
- Resolve missing data, pending queries, and SDV backlogs.
- Conduct subject-level data reviews to check protocol adherence.
- Identify site-level risks and recommend corrective actions.
- Support technical automation and Excel-based formulations.
- Follow customer-specific requirements in the Statement of Work (SOW).
- IQVIA Hiring Centralized Site Associate
Eligibility Criteria
✅ Experience: 2 – 5 years, with at least 1 year in clinical research.
✅ Regulatory Knowledge: Familiarity with ICH-GCP guidelines & local regulations.
✅ Technical Skills:
- Proficiency in clinical systems (EDC, IXRS, CTMS)
- Advanced Microsoft Office (Word, Excel, PowerPoint)
✅ Soft Skills: Strong communication, problem-solving, and time management.
Why Join IQVIA?
- Global Exposure: Work on international clinical trials.
- Career Growth: Enhance skills in data management & regulatory compliance.
- Innovative Research: Contribute to life-saving healthcare solutions.
- Diverse Work Environment: Collaborate with top industry professionals.
How to Apply?
Interested candidates can apply online through the official IQVIA careers portal before February 14, 2025. IQVIA Hiring Centralized Site Associate
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