IQVIA is hiring a Centralized Monitoring Assistant to support clinical research projects by ensuring compliance with regulatory standards, maintaining study trackers, and assisting in risk identification. This role is crucial in optimizing site performance and ensuring high-quality clinical trial execution.
Key Responsibilities:
✔ Provide administrative support to clinical study management teams (e.g., running reports, maintaining trackers).
✔ Assist in updating systems within project timelines for accurate data analysis.
✔ Prepare i-site packs for assigned studies by compiling necessary reports.
✔ Manage access-related administrative tasks (e.g., processing access requests).
✔ Support Technical Solution Specialists (TSS) with Excel formulations and front-end tasks.
✔ Monitor site performance using Key Risk Indicators (KRIs) and recommend corrective actions.
✔ Participate in Kick-Off meetings, team meetings, and client discussions as needed.
✔ Ensure adherence to the Central Monitoring Plan and regulatory guidelines (ICH-GCP).
Qualifications & Skills:
✅ Graduate/Post Graduate in Life Sciences or related field.
✅ Minimum 2 years of experience (with at least 6 months in a relevant role).
✅ Basic knowledge of ICH-GCP, clinical research regulations, and local guidelines.
✅ Proficiency in Microsoft Office (Word, Excel, PowerPoint).
✅ Strong communication, time management, and problem-solving skills.
✅ Ability to work collaboratively in a team and with clients.
About IQVIA
IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions for the life sciences industry. We accelerate medical advancements by providing intelligent insights, real-world data, and innovative technologies to improve patient outcomes worldwide.
