The Central Monitor plays a key role in data surveillance by overseeing clinical trials through centralized monitoring activities to ensure data quality and patient safety
Job Summary
The Central Monitor plays a key role in data surveillance by overseeing clinical trials through centralized monitoring activities to ensure data quality and patient safety.
This role involves collaboration with cross-functional teams to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice guidelines.
The Central Monitor supports risk identification, assessment, and mitigation throughout the clinical trial lifecycle, leveraging data analytics and risk-based quality management strategies.
Matching Summary
The Central Monitor plays a key role in data surveillance by overseeing clinical trials through centralized monitoring activities to ensure data quality and patient safety.
Skills & Requirements
Must-have
Centralized monitoring strategies
Risk-based monitoring plans
Clinical trial data analysis
Good Clinical Practice (GCP) compliance
Data surveillance platform usage
Clinical trial risk management
Cross-functional collaboration
Nice-to-have
Strong project management skills
Experience with AI and analytics
Understanding team dynamics
Global matrixed environment experience
Therapeutic area knowledge
Continuous improvement mindset
Diversity and inclusion commitment
Key Requirements
University degree in life science, business or operations
≥ 5 years pharmaceutical industry experience
≥ 3 years monitoring experience including central monitoring
Knowledge of RBQM and adaptive monitoring principles