Visit.Org, Inc. is seeking a Milestone One Site Coordinator to support trial sites in accordance with ICH-GCP, ensuring adherence to protocol requirements and timelines.
You will act as the primary liaison between sponsors, CROs, and sites, coordinating monitoring visits and maintaining regulatory documents. The role requires a Life Science degree with at least 3 years in a clinical trial setting, plus an upper-intermediate level of English to operate within a general team and handle fast-paced,
📌 Global Clinical Trial Site Lead (Neuquén)
🏢 Visit.org
📍 Neuquén
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