IQVIA UK is seeking a Centralized Monitoring Lead for a hybrid/home-based position in Poland, responsible for overseeing a centralized monitoring team to ensure project delivery aligns with quality and regulatory standards. The ideal candidate will have significant clinical trial experience, strong leadership skills, and a commitment to patient safety and data integrity
Job Summary
The role provides leadership of the centralized monitoring team to achieve project objectives while optimizing speed, quality, and cost.
Responsibilities include ensuring subject safety, data integrity, and timely escalation of issues in compliance with ICH GCP guidelines.
The position requires managing operational insights, site metrics trending, and acting as a mentor for junior centralized monitoring staff.
Matching Summary
Match Score: 85
IQVIA UK is seeking a Centralized Monitoring Lead for a hybrid/home-based position in Poland, responsible for overseeing a centralized monitoring team to ensure project delivery aligns with quality and regulatory standards. The ideal candidate will have significant clinical trial experience, strong leadership skills, and a commitment to patient safety and data integrity.
Salary
Base: zł146,800.00 - zł272,500.00; Bonus/Equity: Not specified; Benefits: Health and welfare and/or other benefits
Skills & Requirements
Must-have
Centralized monitoring leadership
ICH GCP regulatory compliance
Clinical trial risk mitigation
Subject level data review
Analytics strategy development
Cross-functional team management
Nice-to-have
Advanced analytics proposal skills
Mentoring junior staff capabilities
Strong negotiation and coaching
Cultural awareness in global teams
Proactive problem solving approach
Key Requirements
Bachelor's degree in clinical or life sciences
Minimum 5 years relevant clinical trial experience
Medical degree with minimum 4 years clinical trial experience
In-depth knowledge of ICH GCP and local regulations