Senior Clinical Trial Assistant

IQVIA · Amsterdam At IQVIA, our Clinical Functional Service Partnership (CFSP) model offers the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA. As a Senior Clinical Trial Assistant within Clinical FSP, you'll work closely with cross-functional study teams, contributing to the coordination, maintenance, and oversight of essential clinical trial documentation and processes, ensuring compliance with regulatory requirements and project timelines. Key Responsibilities: Support the management and maintenance of study documentation and tracking systems. Ensure accuracy, completeness, and quality of clinical trial records throughout the study lifecycle. Collaborate with clinical operations teams to coordinate study-related activities and communications. Assist with document preparation, filing, archiving, and quality control activities. Contribute to compliance with applicable regulatory requirements, SOPs, and Good Clinical Practice (GCP). Provide guidance and support to junior team members when appropriate. Participate in process improvement initiatives aimed at enhancing operational efficiency. Requirements: Previous experience in a Clinical Trial Assistant, Clinical Research Coordinator, Study Coordinator, or similar clinical research support role. Minimum 2 years of experience within clinical research. Solid organizational and document management skills. Strong attention to detail and ability to manage multiple priorities. Excellent communication skills in Dutch and English. Good knowledge of Microsoft Office applications. Understanding of ICH-GCP and clinical research processes. If you're looking to build a career in clinical research and want to contribute to studies that improve patient outcomes worldwide, we would love to hear from you.