Senior Clinical Trial Assistant, Sponsor Dedicated
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Job Overview IQVIA is seeking an experienced Senior Clinical Trial Assistant | 2+ Years Experience Required to support the delivery of clinical research projects within a dynamic and collaborative environment. Working closely with cross-functional study teams, you will contribute to the coordination, maintenance, and oversight of essential clinical trial documentation and processes, ensuring compliance with regulatory requirements and project timelines.
Essential Functions
- 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.
Qualifications
- 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/French and English.
- Good knowledge of Microsoft Office applications.
- Understanding of ICH-GCP and clinical research processes.
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