IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions for the life sciences industry. We provide intelligent insights to accelerate medical advancements and improve patient outcomes worldwide. With a strong presence in over 100 countries, IQVIA is at the forefront of innovative healthcare solutions.
🔗 Learn more about IQVIA: https://jobs.iqvia.com
Job Overview
The Assoc Site Report Specialist plays a crucial role in ensuring high-quality clinical research by reviewing Site Visit Reports (SVRs). The specialist ensures compliance with IQVIA SOPs, ICH-GCP guidelines, and regulatory standards, contributing to data integrity, subject safety, and study success.
Key Responsibilities
✔ Review SVRs to ensure compliance with protocols, timelines, and regulatory requirements.
✔ Identify and escalate critical findings to project teams for corrective actions.
✔ Collaborate with Clinical Project Managers (CPMs) to improve report quality and reduce errors.
✔ Track compliance trends and provide feedback to CRAs and line managers.
✔ Coach and mentor CRAs to enhance report accuracy and efficiency.
✔ Support quality improvement initiatives, including data trending and training.
✔ Participate in project meetings to discuss SVR-related issues and trends.
Qualifications & Skills
✅ Bachelor’s degree in Healthcare, Life Sciences, or related field.
✅ 7-8 years of clinical research experience, including 3-4 years in on-site monitoring.
✅ Strong knowledge of GCP, ICH guidelines, and clinical trial processes.
✅ Excellent communication (written & verbal) and time management skills.
✅ Problem-solving mindset with attention to detail.
✅ Ability to work independently and in a global team environment.
✅ Fluent in English (spoken & written).
Why Join IQVIA?
🌍 Global Impact: Work on cutting-edge clinical trials that improve patient care.
📈 Career Growth: Opportunities for professional development and leadership roles.
💼 Inclusive Culture: Collaborative work environment with diverse teams.
🏆 Industry Leader: Be part of a top-ranked CRO with a strong reputation.
How to Apply?
📌 Last Date: June 27, 2025
