Back to jobsServing as the primary liaison between Novo Nordisk, clinical sites, and cross-functional study teams, conducting on-site and remote monitoring visits in accordance with ICH-GCP and regulatory requirements.
Ensuring patient safety and data integrity by monitoring site data, resolving discrepancies, and managing adverse events in full compliance with protocols and regulations.
Overseeing site performance, recruitment progress, retention, and data collection to ensure study timelines and quality objectives are consistently met.
Leading site training and providing continuous support on study protocols, operational procedures, and compliance requirements to ensure high-quality trial execution.
Driving the implementation of Risk-Based Quality Management (RBQM) principles to proactively identify, assess, and mitigate risks throughout study conduct.
Building and maintaining strong relationships with investigators and site staff while acting as an ambassador for Novo Nordisk values.
Identifying and proactively resolving site-level issues to maintain study timelines and data quality, while maintaining accurate trial documentation including the Investigator Trial Master File.
