Study Start-Up Specialist – Timelines & Compliance

31 lug - Milano
Experteer Italy

Experteer 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.

You will optimize eTMF quality, monitor site performance, address delays, and help improve SSU metrics while maintaining documentation accuracy.

BS degree and 2+ years in clinical research required; strong data-driven decision making and proficiency with Microsoft Office.

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