Clinical Trial Assistant

• 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
• Support the successful execution of clinical trials

Explore Senior Clinical Trial Assistant – Sponsor Dedicated at IQVIA. Review requirements and application details.