Clinical Research Associate — Cardio, Vaccine & ID

Merck

Merck in the United States seeks a Site Management professional responsible for performance and compliance of trial sites, ensuring adherence to ICH/GCP and local regulations. You will serve as the primary site contact and oversee all phases of clinical studies, developing new sites and coordinating with sponsor roles to achieve Site Ready. Travel up to 65-75% domestically and internationally, with 2-3 days per week on a typical schedule. #J-18808-Ljbffr Merck

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Vacancy posted 1 day ago

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