FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.
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Ciudad de México
06 oct
FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.
Ciudad de México
Fortrea Clinical Development Mexico seeks a Regulatory Submissions Specialist to liaise with investigative sites during study maintenance and startup activities. You will collect essential documents to support submissions and ensure they are submitted within project timelines, under guidance from senior staff.
You will assist in compiling, reviewing, and obtaining approvals from IRB/IEC/Regulatory Authority, liaise with vendors, and adapt patient-facing materials to country-specific
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📌 Global Regulatory Submissions & Site Activation Associate (Ciudad de México)
🏢 FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.
📍 Ciudad de México
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