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
🎯 Intermedio📄 Tempo indeterminato🏠 In sede🧭 Healthcare🏢 Sanità⏳ 2+ anni🗣️ Italiano
Competenze richieste
gcpichclinical-trial-managementregulatory-submissionssite-readinessadverse-event-reportingproject-management
Pronto a fare il colloquio?
Carica il tuo CV su tailk.me e l'AI farà il colloquio per te.
Crea il tuo AI headhunter e fai il colloquioAnnunci correlati
Account Associate
SITA Switzerland Sarl
Roma, Provincia di Roma
Associate Director, Regional Market Access
Blueprint Medicines
Roma, Provincia di Roma
Associate Director, IT Strategy Consulting, Telco
Gartner
Roma, Provincia di Roma
Associate Director, Commercial Lead Oncology
Bristol-Myers Squibb
Roma, Provincia di Roma
Area Finance - Managemengt Reporting Associate
BNP Paribas
Roma, Provincia di Roma
Associate Manager ERP Package Applications
DXC Technology
Roma, Provincia di Roma
tailk