Job Description
IQVIA is seeking a Clinical Research Associate to perform monitoring and site management for clinical protocols in Mexico City. You'll be responsible for site monitoring visits, evaluating study site practices, and maintaining documentation according to regulatory requirements.
The ideal candidate should have a Bachelor's Degree and at least 5 years of experience in on-site monitoring, with strong knowledge of GCP and ICH guidelines. Excellent communication and organizational skills are essential for collaboration with study team members.
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