Milestone One Site Coordinator in Veracruz, Mexico, offers support to trial sites ensuring adherence to ICH-GCP and protocol-defined timelines. You will act as the main liaison between sponsors/CROs and sites, facilitating enrollment and regulatory processes on-site.
The role demands a Life Science degree, at least 2 years of clinical trials experience, and strong English skills to operate in a general team environment. On-site work in Túxpam de Rodríguez Cano is required.
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📌 Onsite Clinical Research Coordinator — Drive Trial Timelines (Ciudad de México)
🏢 Milestone One
📍 Ciudad de México
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