Senior Clinical Trial Assistant

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.