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Clinical Trials Assistant |
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Summary: CLINICAL TRIALS ASSISTANT Duties: * Assist with the preparation of all clinical study documents (e.g. protocol, CRFs, forms and manuals) and presentation material. * Supports and assists with study site management, including liaising with site staff * Assist with IRB submission preparation and study site set up for initiation * Support with the organization of investigator meetings * Manage the set-up, maintenance and archiving of Trial Master File documents. Establish and maintain file systems. * Assist with shipping, inventory, reconciliation of study ... Category: Pharmaceutical | |