Study Start-Up Specialist – Timelines & Compliance

01 ago - Milano
Experteer Italy

pExperteer Italy is seeking a Site Start-Up Specialist to lead initiation of clinical trials, ensuring regulatory compliance and timely site activation in collaboration with study startup teams, CROs and Clinical Operations. /ppYou will optimize eTMF quality, monitor site performance, address delays, and help improve SSU metrics while maintaining documentation accuracy. /ppBS degree and 2+ years in clinical research required; strong data-driven decision making and proficiency with Microsoft Office. /p #J-18808-Ljbffr

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