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Parexel is seeking an organized Trial and Site Administration professional in the United States to support administrative tasks across clinical studies from start-up to closeout. The role involves coordinating with CRAs, LSAD, and vendors, managing documentation, and ensuring compliance with ICH-GCP and local requirements. The candidate will handle eTMF/ISF maintenance, meeting preparations, and regulatory submissions, contributing to efficient trial execution and inspections readiness.

Also on the board Same function, level within a rung

Level

Senior

Location

New York, NY

Occupation

Clinical Research Coordinators

Industry

Research and Development in the Physical, Engineering, and Life Sciences

Posted

yesterday

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