OPIS s.r.l. seeks a Clinical Research Associate to manage and monitor multi-country clinical trials in alignment with study protocols and ICH-GCP.
You will oversee site selection, initiation, monitoring, and close-out, ensuring data quality and patient safety while reporting to the Clinical Project Manager. Responsibilities include feasibility studies, site visits, data verification, adverse event reporting, and collaboration with sponsors and site staff.
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📌 Clinical Research Associate: Impactful Trial Monitoring (Bathurst)
🏢 OPIS
📍 Bathurst
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