FSP Clinical Trial Coordinator - Site Record Coordination

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an FSP Clinical Trial Coordinator – Site Record Coordination based in India. We are looking for a detail-oriented Clinical Trial Coordinator to support global clinical research operations through effective site documentation management and clinical trial record coordination. In this role, you will oversee the collection, review, tracking, and maintenance of essential study documentation to ensure accurate, timely, and compliant trial execution. You will work closely with clinical study teams, investigators, research sites, and cross-functional stakeholders throughout the study lifecycle, from start-up to closeout. You will also support Trial Master File (TMF/eTMF) activities, clinical systems, regulatory documentation, and site communications. Your contribution will help maintain high-quality study records, improve operational efficiency, and ensure adherence to clinical research standards. This is an opportunity to develop your expertise in international clinical trials within a collaborative and quality-focused environment.