Clinical Trial Site Monitor & Data Integrity Lead
Listed on 2026-10-07
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Science
Clinical Research, Healthcare Compliance
IQVIA is seeking a Site Monitoring professional to ensure that study sites conduct and report data per protocol, regulations, and sponsor requirements. You will perform monitoring visits and coordinate with sites to support recruitment and data quality.
Responsibilities include managing site documents, tracking regulatory submissions, and maintaining TMF/ISF in compliance. Strong English communication and GCP/ICH knowledge are required.
Join us at IQVIA as our next Clinical Trial Site Monitor & Data Integrity Lead in Bellingham, WA, United States.
Step into the Clinical Trial Site Monitor & Data Integrity Lead role at IQVIA in Bellingham, WA, United States and grow with us.
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