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Clinical TrialsiCRO Operations

Site management support for imaging CRO clinical trials

Dedicated project coordinators / site managers supporting imaging CRO squads on investigator site setup, monitoring and document control.

Context

An imaging CRO running multi-site oncology and neurology trials needed additional Project Coordinator / Site Manager capacity to support squad teams on investigator site setup, essential-document collection and study status reporting, without expanding internal headcount.

Objective

Provide trained site-management contractors to handle site initiation and follow-up, essential document collection and validation, internal database updates and status reporting to the Project Manager, in line with the client's SM chapter procedures.

Approach

Life-science graduates with 0–2 years of CRO experience and strong English were selected, onboarded on the client's SM procedures and tooling (Microsoft 365, internal trackers), and embedded in the squad under a Senior Project Manager. Backup coverage across squad activities was activated once training was validated.

Outcome

The imaging CRO scaled its site-management capacity on demand while preserving compliance with its SM good practices, with weekly status reporting to the squad lead and predictable coverage across the portfolio of studies.