Oxford Global Resources is seeking a Clinical Affairs support professional to help ensure study site selection and conduct in compliance with GCP and federal regulations. The role involves on-site monitoring activities and coordination of supplies across study sites, working with the Clinical Affairs team.
The candidate should have 2+ years in clinical research, an RN or biology degree, and knowledge of FDA CFRs.
📌 Clinical Research Associate: Site Monitoring & Compliance (Padova)
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📍 Padova
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