Lead Clinical Research Associate – Site Monitoring (México)

11 jun

Fortrea

México

11 jun

Fortrea

México

Fortrea is seeking a Senior CRA I based in Ciudad de México, who will be responsible for site monitoring, management of clinical studies, and project leadership. The role requires a minimum of three years clinical monitoring experience, with a strong understanding of regulatory requirements and the drug development process.

The successful candidate will work closely with study sites, ensuring compliance with protocols and maintaining data integrity, while also being involved in project management tasks. Travel is a requirement, as the position entails oversight across various clinical sites.

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📌 Lead Clinical Research Associate – Site Monitoring (México)
🏢 Fortrea
📍 México

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Coordinador de Relaciones Institucionales - Educación Superior (México)

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Eadic

México

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Eadic
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