IQVIA is seeking an Experienced Clinical Research Associate, Site to perform monitoring and site management duties needed to ensure studies are conducted according to protocol, GCP, ICH guidelines, and sponsor requirements. You will conduct site visits—from selection to
IQVIA seeks an Experienced Clinical Research Associate to work from home in Italy. You will perform site monitoring and site management to ensure studies are conducted per protocol, GCP, and ICH guidelines. You will coordinate monitoring visits and
IQVIA is seeking an Experienced Clinical Research Associate, Site to perform monitoring and site management duties needed to ensure studies are conducted according to protocol, GCP, ICH guidelines, and sponsor requirements. You will conduct site visits—from selection to
IQVIA seeks an Experienced Clinical Research Associate to work from home in Italy. You will perform site monitoring and site management to ensure studies are conducted per protocol, GCP, and ICH guidelines. You will coordinate monitoring visits and
Clinical Contracts Associate – Italy Location: Remote, Italy – open to candidates based anywhere in Italy Employment Type: Full-Time, 12-Month Fixed-Term Contract Hours: 40 hours per week Start Date: To be confirmed Project Status: Pipeline opportunity, pending
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Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our Milan office. Clinical Trial Managers with expertise
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