Clinical Research Associate: Site Monitoring & Study Oversight
Listed on 2026-10-15
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist -
Healthcare
Clinical Research
IQVIA is seeking an experienced Clinical Research Associate to monitor study sites and ensure data integrity in line with the protocol, regulations, and sponsor requirements. The role requires engaging with sites to drive recruitment plans, administer protocol training, and maintain clear communications throughout the study lifecycle.
The ideal candidate has 2+ years of on-site CRA experience, strong knowledge of GCP/ICH guidelines, and proficiency with EDC, CTMS, and eTMF systems, alongside
Consider building your career as a Clinical Research Associate:
Site Monitoring & Study Oversight at IQVIA.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 75..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Clinical Research Associate:
Site Monitoring & Study Oversight role in the description above.
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