FSP Clinical Trial Coordinator - eTMF

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 – eTMF based in India. We are looking for a detail-oriented Clinical Trial Coordinator to support the planning, execution, and administration of global clinical trials, with a particular focus on electronic Trial Master File (eTMF) management. In this role, you will oversee essential clinical documentation, maintain study records, and support clinical systems to ensure accurate, compliant, and timely trial delivery. You will collaborate closely with clinical study teams, investigators, research sites, vendors, and internal stakeholders throughout the clinical trial lifecycle. Your responsibilities will include supporting study start-up, regulatory submissions, site qualification, and ongoing study activities. You will also contribute to maintaining inspection-ready documentation and ensuring compliance with international clinical research standards. This is an excellent opportunity to develop your expertise in clinical operations and eTMF management within a collaborative, international, and innovation-driven environment.