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Clinical Trial Coordinator - Monitoring (Remote)

Merck • Rahway, NJ, US • published 2026-11-06 00:59:38.726270

Description

Job Description Under the oversight of the line\-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing, and archiving clinical documents. The Clinical Trial Coordinator\-Monitoring (CTC\-M) supports clinical supply and non\-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable. The role is critical to meet planned Site Ready dates, including assisting with the preparation of submission packages to IRB/ERC and Health Authorities. The role will collaborate at local level closely with Clinical Operations Manager (COM), Clinical Research Manager (CRM) and Clinical Research Associate (CRA). And the person collaborates with finance/budgeting representatives to manage Clinical Trial Research Agreement (CTRAs) and payments. **Responsibilities include, but are not limited to:** * Trial and site administration: * Provide expert assistance with data tracking and reporting tasks to various teams within the Site Management \& Monitoring organization * Ensure collation and distribution of study tools and documents * Update clinical trial databases (CTMS) and trackers * C...

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