Milan Study Startup Specialist I — Site Activation

In this role you will drive study startup activities to ensure timely activation of clinical sites in Italy. You will partner with project teams, sites, vendors, and review bodies to streamline ethics, regulatory submissions, and site activation. You’ll monitor startup timelines, optimize processes, and contribute to a global pharmacovigilance-minded...

In this role you will drive study startup activities to ensure timely activation of clinical sites in Italy. You will partner with project teams, sites, vendors, and review bodies to streamline ethics, regulatory submissions, and site activation. You’ll monitor startup timelines, optimize processes, and contribute to a global pharmacovigilance-minded...

OverviewIn this role you will drive study startup activities to ensure timely activation of clinical sites in Italy. You will partner with project teams, sites, vendors, and review bodies to streamline ethics, regulatory submissions, and site activation. You'll monitor startup timelines, optimize processes, and contribute to a global pharmacovigilance-minded...

Psi CRO is seeking a Study Start-Up coordinator in the Milan area to drive activation of clinical sites in Italy.Esperienza, qualifiche e soft skill: possiede tutti i requisiti per avere successo in questa opportunità? Lo scopra qui sotto.You will partner with project teams, sites, vendors, and review bodies to streamline ethics, regulatory submissions, and...

In this role you will drive study startup activities to ensure timely activation of clinical sites in Italy. You will partner with project teams, sites, vendors, and review bodies to streamline ethics, regulatory submissions, and site activation. You’ll monitor startup timelines, optimize processes, and contribute to a global pharmacovigilance-minded...

SmartRecruiters, Inc. is seeking a Study Startup Specialist in Milan to support clinical projects in Italy. This hybrid role partners with project teams to ensure startup activities start smoothly and on time. You will collect regulatory documents, prepare site packages, negotiate site contracts and budgets, and coordinate communication with investigators,...

Overview In this role you will drive study startup activities to ensure timely activation of clinical sites in Italy. You will partner with project teams, sites, vendors, and review bodies to streamline ethics, regulatory submissions, and site activation. You’ll monitor startup timelines, optimize processes, and contribute to a global...