Associate Centralized Monitoring Lead
IQVIA · Sofia, Bulgaria
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Role summary
This role supports centralized monitoring leads on clinical trial projects, collaborating across functional teams to deliver sponsor objectives while maintaining quality and compliance. Responsibilities include reviewing monitoring plans, managing study metrics and analytics, escalating clinical risks, and assisting with operational oversight from study initiation through closeout. The position requires adherence to ICH/GCP guidelines, SOPs, and regulatory standards to ensure data integrity and subject safety.
What they're looking for
- Bachelor's degree in clinical or life science field
- Experience supporting centralized monitoring activities in clinical trials
- Knowledge of ICH/GCP guidelines and regulatory compliance requirements
- Proficiency with clinical data review and quality assurance processes
- Strong organizational skills for managing study documentation and tracking systems
What you'll be doing
- Support CMS leads on clinical deliverables aligned with protocol and regulatory guidelines
- Develop and implement monitoring strategies including triggers, thresholds, and analytics
- Review site visit reports, identify issues, and escalate to clinical leadership
- Conduct periodic site performance evaluations and key risk indicator assessments
- Manage study metrics, trends, and cross-functional team coordination for milestone achievement
Privacy & handoff
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