Global Site Start-Up & Regulatory Specialist
FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.
Fortrea is seeking a Regulatory Start-up Specialist to act as the local expert for site activation and regulatory submissions. You will collect essential documents, prepare country applications, and liaise with EC/IRB/Regulatory Authorities to meet timelines and sponsor requirements.
The role requires 2+ years in clinical research with strong ICH/RA/IRB knowledge and the ability to train less-experienced colleagues. Office-based in Mexico City with cross-country coordination.
#J-18808-LjbffrVacante publicada el 1 día atrás
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