ICON plc

Key responsibilities include:
Study Design – serve as a technical expert to CST for vendor selection, budget and timeline estimates
Study Set-Up – translate protocol requirements into vendor technical specifications; liaise with procurement for vendor proposal, budget and contract
Study Initiation – review and finalize vendor plans, manuals and tools; oversee UAT completion; ensure finalization of vendor requirements on time
Study Management – monitor the collection, processing, and analysis of data; evaluate vendor compliance and data quality, manage budget revisions throughout study
Quality / Issue Management – serve as primary PoC for vendor issue escalation; track corrective actions in relation to issues and audit findings
VET Support – provide analysis and reporting of cross-project trends, issues and risks
Vendor Management Infrastructure – develop tools, processes and reports which simplify and standardize CST / vendor interface

Must have Clinical Research/Pharma experience
Must have Fluent English