Onsite Clinical Research Associate — Sponsor-Focused Monitoring

IQVIA

IQVIA invites applications for a site monitoring role based in the United States. You will ensure that clinical sites conduct studies per protocol, GCP, and sponsor requirements, coordinating training and communications with site staff. Responsibilities include monitoring visits, recruitment tracking, data query resolution, and TMF/ISF documentation maintenance to support trial integrity and timelines. #J-18808-Ljbffr IQVIA

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Vacancy posted 1 day ago

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IQVIA
Afton, WY
1 day ago

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