Clinical Trial Management Associate

Responsibilities

• Set up and maintain the site level TMF/eTMF, coordinate on document collection, upload into SharePoint (SP)/eTMF, check document completeness, and provide TMF/eTMF quality control (QC) if required.
• Coordinate EC submission dossier, site start‑up preparation, and EC fee application and tracking.
• Process protocol amendments; may include ICF updates.
• Collect and update study trackers/metrics report for site level if needed.
• Assist in contract signature process; assist in site level payment initiative and payment and invoice tracking.
• Distribute site materials and equipment, document printing, shipment, and other administrative work.
• Business and department office administration support if required.
• Undertake other reasonably related duties as may be assigned from time to time, appropriate for level of experience.

Essential Functions

• Set up and mainta...

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