Senior Clinical Research Monitor — On-Site Protocol Expert
Listed on 2026-10-20
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Research/Development
Clinical Research, Research Scientist, Medical Science
IQVIA is seeking an on-site Clinical Monitor to ensure that study sites conduct the protocol and report data in compliance with GCP, ICH guidelines and sponsor requirements. Travel to diverse sites will be required for monitoring visits.
Responsibilities include site selection, initiation, monitoring, training, recruitment tracking, TMF/ISF maintenance, and collaboration with the study team. A bachelor's degree and 3+ years of monitoring experience are preferred.
We have an opening for a Senior Clinical Research Monitor — On-Site Protocol Expert in Carlsbad, CA, United States within Bio & Pharmacology & Health, Management & Operations.
This position is for the Senior Clinical Research Monitor — On-Site Protocol Expert role at IQVIA Argentina.
We are seeking a motivated Senior Clinical Research Monitor — On-Site Protocol Expert to join IQVIA Argentina in Carlsbad, CA, United States.
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