About the role

IQVIA seeks a Centralized Monitoring Assistant to support clinical study management teams in Thane and Pune. The role involves providing administrative assistance, maintaining study trackers, and monitoring site performance metrics under supervision. This full-time position requires adherence to Good Clinical Practices and regulatory standards.

What you’ll do

Provide study-level administrative support including running reports and maintaining trackers
Assist in updating systems and driving tracking compliance for credible data analysis
Prepare i-site packs by pulling associated reports for respective sites and countries
Process access requests and follow up with vendors for project execution support
Review site-level Key Risk Indicators (KRIs) and historic performance per the Central Monitoring Plan
Identify site-level risks/issues and recommend timely corrective actions
Review effectiveness of recommended actions and take additional steps if needed
Attend kick-off, weekly team, and client meetings as requested

What you’ll bring

Minimum 2 years of work experience with at least 6 months relevant experience
Graduate or Post Graduate degree in Life Sciences or equivalent
Basic knowledge of Good Clinical Practice (GCP) and local regulations
Proficiency in Microsoft Word, Excel, and PowerPoint

Skills

Clinical Study ManagementGood Clinical PracticeMicrosoft ExcelData EntrySite Performance MonitoringRisk IdentificationWritten CommunicationTime Management

Education

Other Graduate/Post Graduate in Life Sciences or educational equivalent.