Sponsor CRA — On-Site Monitoring & Site Leadership
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Research/Development
Job Description & How to Apply Below
IQVIA is seeking an experienced Clinical Research Associate to monitor study sites and ensure compliance with the protocol, regulations, and sponsor requirements. The role includes site visits, site training, recruitment tracking, and documentation management.
The candidate should have at least 2 years of independent on-site CRA experience, strong knowledge of GCP/ICH, and proficiency with EDC/CTMS/eTMF systems.
Are you ready to take on the Sponsor CRA — On-Site Monitoring & Site Leadership role at IQVIA Inc?
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 Sponsor CRA — On-Site Monitoring & Site Leadership role in the description above.
We appreciate your interest in this position.
Join IQVIA Inc and contribute to our ongoing work.
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