Demonstrate understanding of study protocols and essential docs (CMP, IB, ICFs, eCRFs).
Coordinate Site Selection, Initiation, and Close-Out Visits with trial teams.
Serve as primary contact for interim analysis, database locks, and major milestones.
Lead monitoring operational strategy from start-up through close-out.
Ensure monitoring deliverables progress on time, within scope and budget.
Oversee design and maintenance of documents such as CMP, eCRFs, SOPs, WIs.

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