IQVIA Inc is seeking an Associate Centralized Monitoring Lead in Poland to oversee centralized monitoring activities for clinical studies, ensuring adherence to regulations and quality standards. The ideal candidate will have experience in clinical research and strong communication skills, working in a hybrid environment
Job Summary
Lead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout.
Ensure subject safety, data integrity, escalation of issues and timely and responsive feedback in compliance with IQVIA SOP, ICH/ GCP guidelines, protocol requirements and regulatory compliance.
Provide Mentorship to central monitors and CMA centralized monitoring associates and act as subject matter expert on one or more CMS specific activities/deliverables.
Matching Summary
Match Score: 85
IQVIA Inc is seeking an Associate Centralized Monitoring Lead in Poland to oversee centralized monitoring activities for clinical studies, ensuring adherence to regulations and quality standards. The ideal candidate will have experience in clinical research and strong communication skills, working in a hybrid environment.
Salary
Base: zł102,800.00 - zł190,900.00; Bonus/Equity: Not specified; Benefits: Not specified
Skills & Requirements
Must-have
Centralized monitoring activities
Clinical study management
Review structured clinical data
Subject level data review
Remote monitoring visits
Site visit report review
ICH/GCP guidelines adherence
Site level KRI review
Clinical operations plan compliance
Nice-to-have
Mentorship to central monitors
Subject matter expert
Automation of ISP
Process enhancements
Work across cultures and geographies
Key Requirements
Minimum 1.5 yrs of Central Monitoring or Risk-based quality management Experience
Bachelor's Degree Clinical, life sciences, mathematical sciences, or related field, or nursing qualification