17 oct
|
FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.
|
Ciudad de México
17 oct
FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.
Ciudad de México
Fortrea is seeking a Clinical Research Associate to monitor investigation sites in accordance with ICH GCP, SOPs, and sponsor requirements. You will verify informed consent, ensure data integrity, track regulatory documents, and manage trial materials with rigorous quality control.
Travel is a core aspect of the role to conduct on-site visits. The role requires a university degree in a related field, 2 years of monitoring experience, and fluency in English.
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📌 Lead CRA: Clinical Monitoring & Site Trials Specialist (Ciudad de México)
🏢 FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V.
📍 Ciudad de México