Clinical Study Manager I
Dm Clinical Research Group
Dm Clinical Research Group seeks a Study Manager I to oversee clinical operations at assigned investigative sites, ensuring adherence to sponsor protocols, FDA regulations, and ICH-GCP guidelines. You will drive training, monitor enrollment, and maintain essential study documentation. Responsibilities include ALCOA-C compliance, SAE reporting, data quality, and cross-functional coordination to meet sponsor expectations and timelines. #J-18808-Ljbffr Dm Clinical Research Group
Vacancy posted 3 days ago
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