Virtustant is seeking a Clinical Trial Coordinator II to support site activation activities and regulatory submissions for investigative sites in a dynamic pharmaceutical operations environment. The role requires coordination with the Project Team, completion of regulatory and ethics documents, and timely management of site file reviews and communication with sites.
A bachelor’s degree in life sciences and 1+ year of clinical research experience are preferred, with advanced English required.
📌 Clinical Trial Site Activation Coordinator (Santa Fe)
🏢 Virtustant
📍 Santa Fe
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