IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Committed to driving healthcare forward, IQVIA delivers innovative solutions that help accelerate clinical development, improve patient outcomes, and optimize commercialization strategies.
With a strong presence in over 100 countries, IQVIA empowers healthcare organizations with data-driven insights and cutting-edge research methodologies. Join a dynamic team dedicated to making a meaningful impact on global healthcare.
Job Description: Associate Site Report Review
Key Details:
- Position: Associate Site Report Review
- Experience: 3-5 years
- Location: Remote
- Work Mode: Hybrid
- Key Skills Required: CRA (Clinical Research Associate), Site Report Review, Site Monitoring
Key Responsibilities:
- Conduct thorough review and analysis of site reports to ensure compliance with protocols, regulations, and company standards.
- Collaborate with clinical research teams to monitor site activities and data integrity.
- Identify discrepancies, risks, and areas for improvement in site reports.
- Ensure timely and accurate documentation of site monitoring visits and findings.
- Maintain strong communication with investigators, site staff, and internal stakeholders.
- Support audit readiness and regulatory inspections as needed.
Desired Skills & Qualifications:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field.
- 3-5 years of experience in clinical research, preferably as a CRA or in site monitoring.
- Strong understanding of ICH-GCP, regulatory guidelines, and clinical trial processes.
- Excellent analytical, organizational, and communication skills.
- Ability to work independently in a remote/hybrid setup.
How to Apply?
If you meet the qualifications and are excited about this opportunity, send your updated resume to:
📧 Email: navitha.gouli@iqvia.com
Join IQVIA and contribute to shaping the future of healthcare innovation!
