Sponsor-Focused Clinical Research Associate
IQVIA
IQVIA is seeking a Site Monitor to oversee study sites in New Jersey, ensuring data are reported per protocol and regulatory standards. You will conduct visits and coordinate with sites under GCP guidance. Role requires at least 2 years of on-site monitoring, strong English communication, and solid knowledge of GCP/ICH guidelines. This position involves training sites, managing regulatory submissions, and maintaining TMF/ISF records. #J-18808-Ljbffr IQVIA
Vacancy posted 4 days ago
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