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Monitor drug and ancillary supplies to ensure adequate stock at study sites.

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Consolidate dosing data from electronic sources to ensure compliance with patient dosing.

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Track clinical trial insurance and licensing agreements, coordinating with vendors to keep them updated.

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Manage the internal approval process for contracts, purchase orders, and change orders.

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Oversee Clinicaltrials.gov postings and coordinate translations of study documents.

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Develop and maintain internal and external tracking tools.

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Support the development and review of study documents.

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Perform TMF quality checks and coordinate study-specific training.

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Organize meetings and prepare meeting minutes.

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Support the planning and organization of Investigator Meetings.

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Review site monitoring reports.