These roles are accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company’s policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, Head COMs or CRD, the person is responsible for diverse aspects, for execution and oversight of clinical trial country submissions and approvals and to ensure Site Ready. Responsibilities inc…
Associate Clinical Operations Manager I
MSD
IT
🎯 Mid-level📄 Permanent🏠 On-site🧭 Healthcare🏢 Healthcare⏳ 2+ yrs🗣️ Italian
Required skills
gcpichclinical-trial-managementregulatory-submissionssite-readinessadverse-event-reportingproject-management
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