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Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site monitoring across the Midwest. You will partner with investigative sites, study teams and sponsors to ensure data quality and patient safety, from site qualification through closeout.
You will travel regionally (about 8–10 days per month) and bring 5+ years of CNS trial monitoring experience, guiding regulatory compliance and study success in a dynamic CRO setting.
Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site monitoring across the Midwest. You will partner with investigative sites, study teams and sponsors to ensure data quality and patient safety, from site qualification through closeout.
You will travel regionally (about 8–10 days per month) and bring 5+ years of CNS trial monitoring experience, guiding regulatory compliance and study success in a dynamic CRO setting.