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IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions for the life sciences industry. With a focus on accelerating medical advancements, IQVIA provides intelligent insights to improve patient outcomes worldwide. Learn more at IQVIA Careers.
Detailed Job Description
Job Title: Associate Site Report Specialist
Key Responsibilities:
- Review Site Visit Reports (SVRs) to ensure compliance with ICH-GCP, SOPs, and protocol requirements.
- Track corrective/preventive actions (CAPA) to maintain data integrity and subject safety.
- Collaborate with Clinical Project Managers (CPMs) to improve report quality and reduce errors.
- Identify trends in CRA/site performance and escalate risks to project teams.
- Provide coaching and training to CRAs to enhance report accuracy.
- Support quality improvement initiatives, including data trending and mentoring junior staff.
Essential Skills & Qualifications:
- Strong knowledge of clinical research processes, GCP, and regulatory compliance.
- Experience in SVR review, clinical monitoring, or quality assurance roles.
- Analytical mindset with attention to detail.
- Excellent communication and problem-solving skills.
Eligibility & Requirements
✅ Bachelor’s/Master’s in Life Sciences, Pharmacy, or related field.
✅ 4 – 6 years of experience in clinical research, site monitoring, or quality review.
✅ Familiarity with clinical trial documentation and risk-based monitoring.
Benefits of Working at IQVIA
✔ Competitive salary & performance bonuses
✔ Health & wellness programs
✔ Career growth & professional development
✔ Flexible work policies
✔ Global exposure in clinical research
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How to Apply
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