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Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee multi-site monitoring activities across the Midwest region. The role emphasizes data quality, patient safety, and regulatory compliance, including leadership across trial activities.
You will partner with investigative sites, study teams and sponsors, traveling 8–10 days per month to ensure protocol adherence and timely data collection throughout the trial lifecycle.
Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee multi-site monitoring activities across the Midwest region. The role emphasizes data quality, patient safety, and regulatory compliance, including leadership across trial activities.
You will partner with investigative sites, study teams and sponsors, traveling 8–10 days per month to ensure protocol adherence and timely data collection throughout the trial lifecycle.