Study Start-Up
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Parexel International is seeking a Site Activation Partner to lead or support operational activities from study start-up to close-out for assigned sites, ensuring compliance with ICH/GCP, sponsor standards, and study timelines.
Responsibilities include initiating and coordinating documents for the Investigator Initiation Package (IIP), resolving site issues, coordinating with regulatory groups, updating clinical trial systems, and proactive site performance monitoring.